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Product: Milk

Updated: September 23, 2020 9:00 AM

September 23, 2020 9:00 AM

“Report date: Sep 21, 2020
2. City of chicago food service sanitation certificate
- comments: observed no city of chicago certified food manager on site during this inspection while (tcs foods) pork etc. Has been prepared and served. Instructed a city of chicago certified food manager must be on... See Moresite at all times while (tcs foods) are being prepared and served. Priority foundation violation 7-38-012, citation issued.

16. Food-contact surfaces: cleaned & sanitized
- comments: observed a slight debris accumulation on the interior of the ice machine. Must remove debris, detail clean inside ice machine and maintain ice machine at all times.

37. Food properly labeled; original container
- comments: instructed to provide labels for bulk food containers/bins identified with common name (salt, sugar, flour etc).

47. Food & non-food contact surfaces cleanable, properly designed, constructed & used
- comments: observed a torn door gasket inside of the rear 2 door stand-up freezer. Management instructed to replace the torn door gasket.

49. Non-food/food contact surfaces clean
- comments: instructed to detail clean excessive grease build-up on pipes behind cooking equipments and maintain.

51. Plumbing installed; proper backflow devices
- comments: observed water leaks at base of faucet 3-compartment sink. Must repair plumbing leaks and to maintain.

55. Physical facilities installed, maintained & clean
- comments: instructed to replace broken (floor tiles) in front of the 3-compartment sink area.

55. Physical facilities installed, maintained & clean
- comments: instructed to detail clean and organize rear dry storage area and remove unnecessary articles/milk crates due to potential pest harborage.

56. Adequate ventilation & lighting; designated areas used
- comments: instructed to detail clean and maintain kitchen exhaust hood/filters to remove accumulation of grease build-up.

60. Previous core violation corrected
- comments: previous core violation not corrected from inspection report#2352251 dated:11/25/2019 58 2-102. 13 observed the certified food manager without an allergen training certificate. Management instructed that all certified food managers must show proof of training. 02/18/2020 instructed manager to comply with food allergen training and maintain. Priority foundation violation 7-42-090,citation issued.

Source: chicago.gov
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Reported By SafelyHQ.com User

September 21, 2020 5:00 PM

“Company name: GHSW, LLC
Brand name: Trader Joe’s
Product recalled: Southwest Style Sweet Potato Saute Bowl
Reason of the recall: Undeclared milk and egg
FDA Recall date: September 21, 2020
Recall details: GHSW, LLC. is voluntarily recalling 1512 units of Trader Joe’s Southwest Style Sweet Pot... See Moreato Sauté Bowl due to undeclared milk and egg allergens in the dressing that are not declared on the label.  People who are allergic to milk and eggs run the risk of serious or life-threatening allergic reaction if they consume this product.

The dressing is located in a pouch found inside the clear 21.5 oz. bowl. These bowls are sold in the refrigerated section of the store. The recalled product(s) were shipped to 36 Trader Joe’s stores in the following states:  AR, CO, KS, LA, NM, OK, TN, and TX. The recall has been isolated to only Southwest Style Sweet Potato Sauté Bowl with the Best By dates 09/23/20, 09/24/20, 09/25/20, 09/26/20, and 09/28/20 on the front of the package.

No other products or lots are affected by this recall. No reports of illnesses or injury have been received to date. The recall was initiated after it was discovered that the dressing containing milk and egg was distributed in packaging that did not declare the presence of milk or egg. GHSW, LLC is urging customers with any milk and egg allergy concerns to return the product to the point of purchase for a full refund or dispose of the recalled products.  GHSW is standing by to answer customer questions at 888-449-9386, M-F, 9 am to 4 pm PST.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

September 16, 2020 9:00 AM

“Report date: Sep 14, 2020
3. Management, food employee and conditional employee; knowledge, responsibilities and reporting
- comments: observed no written employee health policy on the premises. Management instructed to provide a signed employee health policy for employees. Priority foundation v... See Moreiolation 7-38-010,no citation issued.

5. Procedures for responding to vomiting and diarrheal events
- comments: observed no procedure/plan for responding to vomiting and diarrheal events. Instructed to provide and maintain required procedure/plan and appropriate supplies or kit. (necessary items at a minimum: gloves, face masks, disposable mops and appropriate sanitizer/spray that is effective against norovirus). Priority foundation violation 7-38-005,no citation issued.

10. Adequate handwashing sinks properly supplied and accessible
- comments: observed no hand washing sink located at rear next to the 3-compartment sink. Must install and maintain hand sink supplied with hot and cold running water with soap and hand paper towels. Priority foundation violation 7-38-030(c),no citation issued. .

36. Thermometers provided & accurate
- comments: instructed to provide visible thermometers in all refrigeration units and maintain at all times.

37. Food properly labeled; original container
- comments: prepackaged foods (pastries,sweet treats etc) on display not properly labeled. Must label packages with food name, ingredients, net contents, source and list of allergens. Priority foundation violation 7-38-005,no citation issued.

38. Insects, rodents, & animals not present
- comments: observed approximately 40 rodent (mice) droppings on the cluttered floor under the milk crates being used for storing articles along the west wall grocery isle and around the cluttered rear hot water tank location and in the office space. Management instructed to clean and sanitize all affected areas in detail. Additional pest control service is needed to eliminate the pest activity. Priority foundation violation 7-38-020(a),citation issued.

38. Insects, rodents, & animals not present
- comments: observed damaged weather strip with gap at bottom right corner at front entrance door. Must make and maintain door tight fitting all across the bottom to prevent pest entry.

47. Food & non-food contact surfaces cleanable, properly designed, constructed & used
- comments: instructed not to use milk crates for elevation to prevent hiding places for pests. Must provide appropriate shelving for storage. All food items must also be stored 6' away from the wall for easier cleaning and to maintain.

47. Food & non-food contact surfaces cleanable, properly designed, constructed & used
- comments: observed missing sink stoppers for the dish washing 3- compartment sink. Instructed to provide 3 adequate working sink stoppers and to maintain.

49. Non-food/food contact surfaces clean
- comments: instructed to detail clean interiors of coolers and storage racks and front counter service area to remove food splashed debris and to maintain.

53. Toilet facilities: properly constructed, supplied, & cleaned
- comments: observed no covered waste receptacle provided in the unisex washroom. Must provide.

55. Physical facilities installed, maintained & clean
- comments: instructed to detail clean floors behind under and around refrigeration units behind front service counter and cluttered rear 3 compartment sink/hot water tank area and office space area and to maintain.

55. Physical facilities installed, maintained & clean
- comments: observed cluttered conditions at the rear 3 compartment sink/dry storage area. Instructed to detail clean, organize and/or remove all unnecessary articles to prevent hiding places for pests.

Source: chicago.gov
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Reported By SafelyHQ.com User

September 16, 2020 9:00 AM

“Report date: Sep 14, 2020
10. Adequate handwashing sinks properly supplied and accessible
- comments: instructed to provide hand washing signage at all hand sink in all washrooms. (first/second and third floor)

47. Food & non-food contact surfaces cleanable, properly designed, constructed &... See Moreused
- comments: instructed to repair/replace rubber gasket around walk-in freezer door (noted heavy ice build-up inside walk-in freezer).

47. Food & non-food contact surfaces cleanable, properly designed, constructed & used
- comments: instructed to properly use shelves 6' off the floor inside walk-in cooler and in rear storage room for easy access on cleaning. No milk crates.

52. Sewage & waste water properly disposed
- comments: found 3 compartment sink not properly maintained. Waste water backing up from one compartment into another compartment of the 3 compartment sink. Instructed to repair priority violation 7-38-030 (c) no citation issued issued 2 day notice

55. Physical facilities installed, maintained & clean
- comments: instructed to detail clean and maintain wall vent cover with excessive grease accumulation above/behind ovens in the kitchen area.

Source: chicago.gov
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Reported By SafelyHQ.com User

September 13, 2020 8:47 PM

“The FSIS announced the recall of approximately 429-lbs of fully-cooked meat sausage products by Cher-Make Sausage Company due to misbranding and an undeclared allergen. The product contains milk (cheese), which is not declared on the packaging label. There have been no confirmed reports of adverse r... See Moreeactions due to consumption of these products to date.

FSIS advises consumers not to eat the recalled products and to throw them away or return them to the place of purchase. The product was produced on July 23, 2020. The products subject to recall bear establishment number “EST. 2420” inside the USDA mark of inspection. These items were shipped to retail locations in Illinois, Minnesota, Nebraska, North Dakota, South Dakota, and Wisconsin and may have been sold intact or from a counter display as individual sausages. The following products are subject to recall:

- 5-lb. vacuum sealed packages labeled as “OLD FASHIONED WIENERS COURSE GROUND FULLY COOKED” with sell by date “11/26/20” and lot number “2020503” on the product label.

Check the full recall details on the FSIS website fsis.usda.gov

Source: FSIS
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Reported By SafelyHQ.com User

September 7, 2020 8:36 PM

“The CFIA announced the recall of Frank brand Milk Chocolate Covered Raisins by Canadian Tire Corporation of Canada from the marketplace due to undeclared peanut.

- Frank Milk Chocolate Covered Raisins (300 g). UPC: 6 26394 33920 7. Best Before 2021 MA 07, Lot: 07EUA | Best Before 2021 MA 13, Lot... See More: 13EUA | Best Before 2021 JL 07, Lot: 07GUB | Best Before 2021 APR 21, Lot: 21DUB | Best Before 2021 JL 08, Lot: 08GUB

Check the full recall details on the CFIA website: inspection.gc.ca

Source: CFIA
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Reported By SafelyHQ.com User

August 18, 2020 7:00 PM

“Company name: SCA Pharmaceuticals
Brand name: SCA Pharma
Product recalled: Heparin Sodium Compounded products
Reason of the recall: Incorrect preservative (benzyl alcohol)
FDA Recall date: August 18, 2020
Recall details: Windsor, CT, SCA Pharmaceuticals (SCA) is voluntarily recalling 10 lots o... See Moref Heparin Sodium to the hospital/user level. The compounded Heparin Sodium bag contains the undeclared preservative benzyl alcohol. The labelling listed methylparaben and propylparaben as preservatives; however, are not present in the product. SCA identified this labeling issue during the investigation of a low potency test result for Heparin Sodium (NDC 70004-0650-46).

Serious adverse reactions including fatal reactions and “gasping syndrome” are likely to occur in premature neonates and low-birth weight infants in the neonatal intensive care unit who receive benzyl alcohol as a preservative in infusion solutions, in any amount. Additional adverse reactions included gradual nervous system deterioration, seizures, bleeding in the skull, blood abnormalities, skin breakdown, liver and kidney failure, low blood pressure, slower than expected heart rate, and loss of sufficient brain blood flow to maintain consciousness.

Preterm, low-birth weight infants may be more likely to develop these reactions because they may be less able to metabolize benzyl alcohol. Furthermore, benzyl alcohol present in mother’s serum is likely to cross into human milk and may be orally absorbed by a nursing infant. For this reason, preservative-free heparin sodium injections is recommended when heparin therapy is needed during pregnancy. Benzyl alcohol is contraindicated in pediatric patients as well as pregnant or nursing women.

SCA has not received any complaints or reports of adverse events to date related to this recall. However, out of an abundance of caution, SCA is voluntarily recalling the lots listed herein. Heparin Sodium is used as an anticoagulant and is packaged in 500 mL or 1000 mL intravenous bags. Check the link below to see the full list of affected Heparin Sodium lots.

The compounded Heparin Sodium can be identified by checking the product name, concentration and lot number on the compounded bag. The compounded Heparin Sodium bags were distributed nationwide to hospitals.

SCA is notifying its customers by certified mail and is arranging for return of all recalled products. Hospitals that have compounded Heparin Sodium bags which are being recalled should stop using the product and return the product to SCA.

Consumers with questions regarding this recall can contact SCA by phone at 877-550-5059 or e-mail customerservice@scapharma.com between the hours of 7:00 am and 7:00 pm (Central Standard Time), Monday through Friday. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

May 29, 2020 8:00 PM

“Company name: PGG/HSC Feed Company, LLC, dba CHS Nutrition
Brand name: CHS Inc.
Product recalled: Champion Meat Goat Pellets R20, Medicated Feed
Reason of the recall: Due to elevated level of Rumensin (monensin)
FDA Recall date: May 29, 2020
Recall details: PGG/HSC Feed Company, LLC, dba CHS... See MoreNutrition of Hermiston, Oregon, is recalling 510 bags (50 lbs. each) of Champion Meat Goat Pellets R20, Medicated Feed due to elevated level of Rumensin (monensin). Monensin is an FDA-approved drug for use in certain animal feeds. However, if the feed contains excessive amounts, the feed can cause monensin toxicity in a number of animal species including goats. Goats ingesting excessive levels of monensin in feed are susceptible to injury and death. In goats, signs and symptoms can include bloated stomach, bloody urine, shortness of breath, muscle weakness or cramps, rapid breathing and death. In humans, monensin could affect handlers of highly concentrated products by causing irritation of the skin, eyes, and respiratory tract through direct exposure.

People or animals who consume meat or milk from animals exposed to very high levels of monensin are at risk of indirect exposure, which could potentially lead to ingestion toxicity.   Champion Meat Goat Pellets R20, Medicated Feed, was distributed to three consignees in Oregon and Washington between April 20, 2020, and April 29, 2020. NW Farm Supply in Hermiston, Oregon and in Prosser, Washington, further sold the recalled product to downstream customers.

The recalled product is pelleted dry feed and bagged in poly bags with the words Payback Champion Feeds printed on the bag. Each bag weighs 50 lbs. The affected lot number 6705 HM928510 04/17/20 and the UPC code 48252 48640 are printed on the tag of each bag. Customers reported that three goats have died, and three additional goats were ill but have recovered to date. The recalled product was found to contain elevated levels of monensin due to a mixing error during manufacturing. The recalled product was put on hold pending testing after a customer complaint. Test results confirmed a higher than expected level and this recall was initiated. CHS Nutrition cannot account for up to 15 bags out of 510 bags distributed to date.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

NBPS cafeteria serving rotten food, North Broward Preparatory School, Lyons Road, Coconut Creek, Florida, USA

North Broward Preparatory School, Lyons Road, Coconut Creek, Florida, USA

April 28, 2020 7:17 PM

“Since last year, which is our first year at North Broward preparatory school, we asked our daughter to stop purchasing food outside of the cafeteria as we pay PLENTY of money for this cafeteria and it is not separated from the TUITION therefore, she is incurring an ADDITIONAL FEE DAILY for alternate... See Morefood which we got hit with last year every month. Over $300 monthly-  we thought our daughter was being a princess until she asked, what does it mean when vegetables look milky?! Omg, we told her that means they’re Rotting... Being a new student she didn’t wanna cause waves so she found an alternate way of eating. February 11 our daughter ate cucumbers.
I have tried to report NBPS cafeteria as it’s poisoned numerous students beginning back in February through the. End of March when all schools closed. The school still has students on campus and I received no updates from the school as to how they’re handling our daughters 2 separate food and chemical poisonings
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Reported By SafelyHQ.com User

Flu like symtoms, Wendy's, 1829 Mangum Road, Houston, TX, USA

Symptoms: Headache Fatigue Body Ache
Wendy's, 1829 Mangum Road, Houston, TX, USA

March 27, 2020 6:34 PM

“I had a milk shake and spice chicken sandwich. The next day I felt really tired and sore like I had the flu. My legs were aching and my head was aching and I felt like I had no energy. This lasted for 24hours I took ibuprofen. then I took some heavy metal detox and after taking the heavy metal det... See Moreox the flue like symtoms completely disappeared. See Less
Reported By SafelyHQ.com User

Recent Interesting Reports

October 28, 2020 11:00 AM

“Company name: Sunstar Americas, Inc.
Brand name: Paroex
Product recalled: Paroex Chlorhexidine Gluconate Oral Rinse, 4 oz and 16 oz
Reason of the recall: Potential contamination with Burkholderia lata
FDA Recall date: October 28, 2020
Recall details: Sunstar Americas, Inc. (SAI) is voluntarily... See Morerecalling Paroex® Chlorhexidine Gluconate Oral Rinse USP, 0.12% products bearing an expiration date from 6/30/22 – 9/30/22 (see specific lots below) to the consumer level. This product may be contaminated with the bacteria Burkholderia lata.

Use of the defective product in the immunocompetent host may result in oral and, potentially, systemic infections requiring antibacterial therapy. In the most at-risk populations, the use of the defective product may result in life-threatening infections, such as pneumonia and bacteremia. To date, no adverse events have been reported to SAI related to this recall. The prescription oral rinse product, available through healthcare professionals only, is indicated for use as part of a professional program for the treatment of gingivitis and is packaged as follows:

- 1789P GUM® Paroex® is distributed in cases each containing 6 amber bottles of 16 fluid ounce (473 ml) chlorhexidine rinse. The bottle has a childproof cap and a 15 ml metered dosage cup, is safety sealed, and is decorated with a multiple-panel wrap-around label.
- 1788P GUM® Paroex® is distributed in cases each containing 24 amber bottles of 4 fluid ounce (118.25 ml) chlorhexidine rinse. The bottle has a childproof cap, is safety sealed, and is decorated with a multiple-panel wrap-around label.

The product can be identified by as shown in the images below: Paroex was distributed Nationwide to Dental offices, Dental distributors, Pharmaceutical wholesalers, Dental schools, and Pharmacies. SAI is notifying its direct distributors and customers by USPS Priority mail and is arranging for return of all recalled products. Patients, pharmacies, and healthcare facilities in possession of these products should stop using and dispensing immediately.

Consumers with questions regarding this recall can contact SAI by phone at 1-800-528-8537 or email us.pcr@us.sunstar.com on Monday-Friday from 8am-5pm CST. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this drug product. Affected products and lot numbers are detailed in the link below.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

October 14, 2020 11:12 PM

“I bought a 4 pack of their Bakery Banana Nut Muffins. I've bought them before, so I didn't have any concerns. On opening my first one, the paper wrapper looked like it had worms on the bottom of it. I'd never seen that before, so I checked the bottom of the muffin, and that had some too. I've thrown... See Morethe rest away. As I said, I've bought these often and they've never had this, so this isn't normal. At this same location, I had gotten a pack of mini brownies in the flat plastic container and there were plastic pieces baked into the brownies. Had to throw those out too, after there were at least 5 with plastic chips in them. Clearly quality control has gone way down here. See Less
Reported By SafelyHQ.com User

October 2, 2020 5:00 PM

“Company name: Ashtel Studios
Brand name: Smart Care
Product recalled: Hand sanitizer packaged in 0.84 oz. pouches
Reason of the recall: Product is packaged in containers resembling a food and drink pouch
FDA Recall date: October 02, 2020
Recall details: Company Announcement Ashtel Studios has a... See Morennounced a voluntary recall of all lots of licensed hand sanitizer packaged in .84 oz containers resembling food and drink pouches labeled with various children’s characters listed in the table below to the consumer level.

The products are being recalled because they are packaged in containers resembling food and drink pouch. The recall does not affect any other Hand Sanitizer products from Ashtel Studios.

Product Size NDC
PAW Patrol Hand Sanitizer 0.84 FL. OZ (25 mL) 70108-042-01
JoJo Siwa Hand Sanitizer 0.84 FL. OZ (25 mL) 70108-044-01
Hot Wheels Hand Sanitizer 0.84 FL. OZ (25 mL) 70108-045-01
Barbie Hand Sanitizer 0.84 FL. OZ (25 mL) 70108-046-01
Trolls Hand Sanitizer 0.84 FL. OZ (25 mL) 70108-047-01
Minions Hand Sanitizer 0.84 FL. OZ (25 mL) 70108-043-01

Ingesting hand sanitizer, which is intended for topical use, could potentially result in alcohol toxicity. Symptoms of alcohol toxicity may range from lack of coordination, slowed or slurred speech, drowsiness to coma, which can be fatal. Furthermore, ingesting alcohol can affect the brain and cause impaired driving or operating heavy machinery. Alcohol can also interact with numerous drugs which may result in serious adverse effects. Ingesting alcohol by people with alcohol addiction may interfere with maintaining abstinence. Additionally, people with alcohol addiction may seek large amounts of ethanol-based hand sanitizers as a substitute. Ashtel Studios has received no reports of adverse reactions.

The product is intended to be applied topically to help reduce bacteria on the skin that could cause diseases when soap and water are not available and is packaged in 0.84 oz pouches. The product can be identified by examples of the products pictured below. Product was distributed to selected retailers in the United States and Canada.

Ashtel Studios has provided written notification to its distributors and retailers and is alerting customers via this voluntary recall. While the product is not available for purchase, if a consumer has product which is being recalled they are advised to destroy it immediately.

Check the full recall details on fda.gov
Source: FDA
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Reported By SafelyHQ.com User

October 9, 2020 12:00 AM

“Company name: Sunshine Mills, Inc.
Brand name:
Product recalled: Pet Food
Reason of the recall: May Contain Aflatoxin
FDA Recall date: October 08, 2020
Recall details: Company Announcement Sunshine Mills, Inc. is expanding its voluntary recall of certain pet food products that were made with c... See Moreorn that contained Aflatoxin at levels above FDA’s action levels. This is an expansion of the recall initiated September 2, 2020, after an investigation conducted along with the U.S. Food and Drug Administration determined that additional corn-based pet food products produced between April 3, 2020 and April 5, 2020 may contain corn from a single load of corn with elevated levels of aflatoxin. Aflatoxin is a naturally occurring mold by-product from the growth of Aspergillus flavus and can be harmful to pets if consumed in significant quantities. No illnesses have been reported in association with these products to date, and no other Sunshine Mills, Inc. pet food products are affected by this announcement.

Sunshine Mills, Inc. has chosen to expand its voluntary recall to include these additional products as a precautionary measure in furtherance of its commitment to the safety and quality of its products. Pets with aflatoxin toxicity (aflatoxicosis) may show symptoms of illness including sluggishness or lethargy combined with a reluctance to eat, vomiting, yellowish tint to the eyes or gums, diarrhea, and in some cases, death. Pets experiencing any of these symptoms after consuming the recalled products should be seen by a veterinarian.

The affected products were distributed in retail stores within the United States. Principle Super Premium Natural Dog Food is exported exclusively to a distributor in Japan. Sportsman’s Pride Maintenance Adult Formula Dog Food is also exported to a distributor in Japan and Colombia. Retailers who received the recalled lots have been contacted and asked to pull any remaining inventory of these lots from their shelves. There are no other Champ®, Field Trial®, Good Dog, Hunter’s Special®, Old Glory®, Paws Happy Life®, Pet Expert, Principle, Retriever®, River Bend, Sportsman’s Pride®, Sprout®, Thrifty®, Top Runner® or Whiskers & Tails products or other lot codes of these products affected by this voluntary recall. The lot codes can be located on the back of each bag.

Consumers who have purchased the recalled products should discontinue use of the product and may return the unused portion to the place of purchase for a full refund. Consumers may contact Sunshine Mills, Inc. customer service at (800) 705-2111 from 7AM to 4PM Central Time, Monday through Friday, or by email at customer.service@sunshinemills.com for additional information. The expansion of this voluntary recall is being conducted with the knowledge of the U.S. Food and Drug Administration. You can see the products affected by this announcement in the link below.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

Unmasked employees, Wintrust Bank - Sauganash, West Peterson Avenue, Chicago, IL, USA

Wintrust Bank - Sauganash, West Peterson Avenue, Chicago, IL, USA

October 12, 2020 6:24 PM

“Walked in. Teller had mask on only over nose. She pulled it up as we approached. The other teller was masked, but this one was reckless and didn't care that co-workers and customers had to breathe in her disgusting breath? I asked a very simple account question and was told to talk to a personal ban... See Moreker. I turned to where she pointed and there sat an unmasked elderly female employee. As I approached her I said put on your mask. She replied that the little plastic partition was enough. I looked at her very shocked and she put on her mask. I refused to sit at her guest chair as it was within about 2 feet of her reckless, unmasked exhaling just moments before. She then immediately took pf her.mask, again putting her co-workers and me at risk, as well as anyone entering. Do they not know about aerosol spread? Needless to say we are closing both we have accounts there. See Less
Reported By SafelyHQ.com User

October 14, 2020 9:00 PM

“Company name: Hadson Toko Trading Co., Inc.
Brand name: Eishindo
Product recalled: Jelly Cups
Reason of the recall: Product poses a choking hazard.
FDA Recall date: October 14, 2020
Recall details: HADSON (TOKO) TRADING CO., INC. OF MASPETH, NY is recalling its 28.2oz (800g) bags of EISHINDO MI... See MoreNI CUP JELLY (50 pcs) (迷你果凍杯(大)) due to the product being a potential choking hazard based off of its product size and consistency. Small jelly cups have previously been implicated in choking deaths of children.

The recalled jelly cups were distributed nationwide in retail food stores and are sold in large clear bags of 50 jelly cups. The UPC code is, “4970481000034,” Product code is, “E007.” No incidents of consumers choking have been reported to date in connection with this product. The potential choking hazard was noted after discussion with a representative from the Food and Drug Administration.

Consumers who have purchased 28.2oz (800g) bags of EISHINDO MINI CUP JELLYS are urged to return them to the store where they were purchased for a full refund or throw them away in a sealed package inside a secure garbage can with a tight fitting lid. Consumers who have questions or concerns may contact the company at 718-628-6761 Monday thru Friday between 8AM and 6PM EST.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

October 22, 2020 7:00 PM

“Company name: COMERCIAL MEXICANA INNTERNATONAL INC
Brand name: TROPIQUE
Product recalled: ASSORTED FRUIT JELLY BAG & JELLY ANIMAL JAR
Reason of the recall: Potential Choking Hazard
FDA Recall date: October 22, 2020
Recall details: FDA Announcement Comercial Mexicana International Inc. in... See MoreBethpage New York is recalling the product because it may pose a choking hazard. Small jelly cups containing seaweed extract (carrageenan) has been identified as a potential choking hazard in children No incidents of consumers choking have been reported to date in connection with this problem. The potential choking hazard was discovered during a routine inspection by the New York State Department of Agriculture and Markets, Food Safety and inspection. The recalled jelly cups were sold in NY, NJ, CT, PA retail stores. The recall products are:
Check the full recall details on fda.gov
Source: FDA
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Reported By SafelyHQ.com User

September 30, 2020 1:00 PM

“Company name: Estado de México, México, DMM VISSION, S.A. de C.V
Brand name: Cleaner
Product recalled: Cleaner Hand Sanitizer
Reason of the recall: Potential Presence of Methanol (Wood Alcohol)
FDA Recall date: September 30, 2020
Recall details: Company Announcement Estado de México, México, D... See MoreMM VISSION, S.A. de C.V. is voluntarily recalling five lots of Cleaner Hand Sanitizer, 500 mL and 1,200 mL plastic clear bottles with white tops currently in US distribution to the consumer level. This recall is being initiated out of abundance of caution due to detection of methanol (wood alcohol) in hand sanitizer sample manufactured at the same facility. Risk Statement: Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system or death. Although all persons using these products on their hands are at risk, young children who accidently ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning. To date DMM VISSION has not received reports of adverse events related to this recall. The product is used as a hand sanitizer and are packaged in 500ml and 1200ml plastic clear bottles with white tops. The lot numbers are LC2020407, LC2020408, LC2020502, LC2020504, LC2020507.  This product was first distributed nationwide to wholesale distributors on April 27, 2020 and finished on June 9th, 2020. The recalled products are as follows:
Check the full recall details on fda.gov
Source: FDA
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Reported By SafelyHQ.com User

October 5, 2020 2:00 PM

“Company name: Marksans Pharma Limited
Brand name: Time-Cap Labs Inc.
Product recalled: Metformin Hydrochloride for Extended-Release Tablets, USP 500 mg and 700 mg
Reason of the recall: Due to the Detection of N-Nitrosodimethylamine (NDMA) Impurity
FDA Recall date: October 05, 2020
Recall detai... See Morels: Marksans Pharma Limited, India is voluntarily expanding its earlier initiated recall on June 05, 2020 to include an additional 76 unexpired lots of Metformin Hydrochloride Extended-Release Tablets, USP 500mg, & 750mg to the consumer level. Marksans performed N-Nitrosodimethylamine (NDMA) testing of unexpired identified marketed lots and observed that NDMA content in some lots is exceeding the acceptable Daily Intake Limit (ADI) of 96ng/day, therefore, out of an abundance of caution, an additional 76 lots are being recalled.

Risk Statement: NDMA is classified as a probable human carcinogen (a substance that could cause cancer) based on results from laboratory tests. NDMA is a known environmental contaminant found in water and foods, including meats, dairy products and vegetables. Marksans Pharma Limited has not received any reports of adverse events that have been related to this recall. Metformin Hydrochloride Extended-Release Tablets, USP 500mg & 750mg are indicated as an adjunct to diet and exercise to improve blood glucose control in adults with type 2 diabetes mellitus and is packaged in HDPE bottles with the following NDC#s in different packing configurations
- Metformin Hydrochloride Extended-Release Tablets, USP 500mg:
90 counts: 49483-623-09
100 counts: 49483-623-01
500 counts: 49483-623-50
1000 counts: 49483-623-10
- Metformin Hydrochloride Extended-Release Tablets, USP 750mg:
100 counts: 49483-624-01

The affected Metformin Hydrochloride Extended-Release Tablets, USP 500mg, are white to off white, capsule shaped, biconvex tablets, debossed with ‘101’ on one side and plain on the other side and Metformin Hydrochloride Extended-Release Tablets, USP 750mg, are white to off white, capsule shaped, biconvex tablets, debossed with ‘102’ on one side and plain on the other side.

Metformin Hydrochloride Extended-Release Tablets, USP 500mg & 750 mg were distributed by Time-Cap Labs, Inc. (located at 7 Michael Avenue, Farmingdale, New York 11735) nationwide in the USA to wholesalers who further distributed to pharmacies.

Marksans Pharma Limited is notifying its distributors and customers by issuing notification letter and press release and is arranging for return/replacement etc. of recalled product lots. Distributors //customers that have affected lots of Metformin Hydrochloride Extended- Release Tablets, USP 500mg & 750mg those are being recalled should return to place of purchase. The lot # can be located on the side panel of bottle labels as well as shipper/case labels.

Consumers with questions regarding this recall and return can contact Ms. Irene McGregor (Vice President, Regulatory Affairs) of Time-Cap Labs, Inc., located at 7 Michael Avenue, Farmingdale, New York 11735, by phone number 631-753-9090; ext. 160, [Monday to Friday 8am-5pm EST] or e-mail address imcgregor@timecaplabs.com.

Consumers taking these recalled product lots of Metformin ER Tablets should continue taking it until a doctor or pharmacist gives them a replacement or a different treatment option. It could be dangerous for patients with type 2 diabetes to stop taking their metformin without first talking to their health care professional. Consumer should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

Check the full recall details and list of products on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Walmart Supercenter, 2240 West Dekalb Street, Camden, South Carolina 29020, USA

Walmart Supercenter, 2240 West Dekalb Street, Camden, South Carolina 29020, USA

October 13, 2020 12:00 PM

“(1) A COVID-19 pandemic plan has not been developed and implemented for employees to include employee wellness checks, disinfecting and sanitizing, social distancing, personal protective equipment, employee return to work and employee training. A manager tested positive for Covid19 and was coming in... See Moreto the store every day of that week.


Source: Osha.gov | Receipt Date: 2020-06-24
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Reported By SafelyHQ.com User