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IMPORTANT - YOUR REPORT IS QUEUED - IT MAY TAKE UP TO 12 HOURS FOR YOUR REPORT TO SHOW ON OUR HOME PAGE (IF NOT OPTED AS PRIVATE)

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Product: Beef

Updated: September 23, 2020 12:00 PM

September 23, 2020 12:00 PM

“Active Covid-19 outbreak of 6 employees at Beef Northwest Feeders in Morrow County. Investigation Start Date: 8/10/20 , with the most recent onset of: 9/12/20 New Cases of: 6

Source: www.oregon.gov See Less
Reported By SafelyHQ.com User

September 23, 2020 9:00 AM

“Report date: Sep 21, 2020
10. Adequate handwashing sinks properly supplied and accessible
- comments: obsreved no soap at hand sink in front prep/cooking area. Instructed must provide hand washing cleanser at all hand sinks at all times. Operator provided during inspection. Priority foundation v... See Moreiolation 7-38-030(c). Citation issued.

10. Adequate handwashing sinks properly supplied and accessible
- comments: observed no paper towels at hand sink in front prep/cooking area, and at hand sink in rear prep area. Must provide sanitary means to dry hands at all hand sinks at all times. Priority foundation volation 7-38-030(c). See above violation 6-301. 11 for citation.

22. Proper cold holding temperatures
- comments: observed tcs foods at improper temperatures in prep cooler in front cooking area. Found beef @ 47. 4f, eggs @ 58. 1f; chicken @ 44. 9; shreded cheese @ 49. 3f; chili rellenos @ 46. 9; cooked vegetables and peppers @ 49. 2f; pork @ 47. 4f ham @ 48. 0f; and pork @ 54. 4f. Instructed must keep all tcs foods @ 41f or less at all times when in refrigeration. Operator voluntarily discarded 40lbs of denature foods during inspection. Operator estimates value to be approximately $200. Priority foundation violation 7-38-005. Citation issued.

23. Proper date marking and disposition
- comments: observed no lables on prepped tcs foods inside coolers and walk in coolers. Must properly label all prepped tcs foods with discard date no more than 7 day from preparation date. Must correct and maintain same. Priority foundation violation 7-38-005. Citation issued.

33. Proper cooling methods used; adequate equipment for temperature control
- comments: found prep cooler not able to maintain proper temperature in front cooking/prep area. Ambient air temperature inside prep cooler @ 50. 0f. Instructed must have ambient air temperature of 41f or less inside all refrigeration. All tcs foods discarded and cooler tagged and held for inspection. Priority violation 7-38-005. Citation issued.

38. Insects, rodents, & animals not present
- comments: found approximately 30 mice droppings on shelves and on floors in basement near stairs. Instructed must eliminate pest issue, must clean and sanitize affected areas. Priority foundation violation 7-38-020(a). Citation issued.

41. Wiping cloths: properly used & stored
- comments: observed used wiping cloths on counters throughout prep areas. Must keep all wiping cloths inside sanitation solution when not in use.

49. Non-food/food contact surfaces clean
- comments: observed excessive grease accumulation on lower interior of fryer. Must detail clean and sanitize. Must maintain same.

55. Physical facilities installed, maintained & clean
- comments: observed cardboard used under matts throughout prep areas. Must remove. All sufraces must be smooth, easily cleanable and nonporous.

Source: chicago.gov
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Reported By SafelyHQ.com User

September 23, 2020 9:00 AM

“Report date: Sep 17, 2020
10. Adequate handwashing sinks properly supplied and accessible
- comments: observed hand-sink in prep area without hand cleanser available for proper hand washing during time of inspection. Instructed to provide and maintain at all times. Priority foundation violation.... See More7-38-030 (c). Citation issued.

10. Adequate handwashing sinks properly supplied and accessible
- comments: observed no hand drying provision available at two handsinks located in (in use) prep area as well as toilet room during time of inspection. Must provide and maintain. Priority foundation violation. 7-38-030 (c). See previous violation for citation.

22. Proper cold holding temperatures
- comments: observed the following time/temperature control for safety food items stored in upright refrigeration unit in prep area at improper cold holding temperatures during time of inspection. They are as follows. . . 5 lbs of cooked beef @163. 0f and 2 lbs of additional beef chunks @ 53. 5f. Instructed to hold all cold held items @ 41f or below at all times and maintain. Manager voluntarily discarded during this time. Priority violation. 7-38-005. Citation issued.

23. Proper date marking and disposition
- comments: observed the following time/temperature control for safety foods stored in cooling units throughout facility without any labels. . . Egg rolls,fried chicken, cooked beef and chicken, marinated chicken/shrimp, and cooked noodles. Instructed to provide discard or use by dates not to exceed 7 days on all food items refrigerated, ready to eat items stored on site for more than 24 hours. Must maintain. Priority foundation violation. 7-38-005. No citation issued.

36. Thermometers provided & accurate
- comments: observed no thermometers inside of both upright refrigeration units located in prep area to to measure internal temperatures. Instructed to provide and maintain.

37. Food properly labeled; original container
- comments: observed working ingredients located at wok without any labels. Must provide common name labels for herbs and spices.

40. Personal cleanliness
- comments: observed dirty aprons worn by all food handlers. Instructed to provide clean outer clothing to wear while open and operating and handling food. Must maintain.

41. Wiping cloths: properly used & stored
- comments: observed soiled wiping cloths stored throughout prep area on tables and hanging on sinks improperly drying. Instructed to store inside sanitizing buckets with chlorine @ at least 50 ppm. Must maintain.

47. Food & non-food contact surfaces cleanable, properly designed, constructed & used
- comments: observed grocery bags used for storage. Instructed to discontinue use and provide food grade storage bags only for food storage. Must maintain.

48. Warewashing facilities: installed, maintained & used; test strips
- comments: observed no chemical test strip kit on site to match available sanitizer (chlorine bleach) for proper sanitizing of equipment/utensils at 3 compartment sink. Instructed to provide and maintain chlorine test strips at all times. Priority foundation violation. 7-38-005. Citation issued.

57. All food employees have food handler training
- comments: observed no food handler training certificates on site for review. Instructed to meet requirements.

58. Allergen training as required
- comments: observed no allergen training for new city of chicago certified food manager on site. Instructed to meet requirement and maintain on site for review.

Source: chicago.gov
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Reported By SafelyHQ.com User

September 15, 2020 12:00 PM

“One employee at Kelly's Roast Beef located on Revere Beach Boulevard in Revere tested positive for COVID-19.

Source: wcvb.com See Less
Reported By SafelyHQ.com User

1 employee tested positive for Covid-19, Kelly's Roast Beef, 410 Revere Beach Blvd, Revere, MA 02151, United States

Kelly's Roast Beef, 410 Revere Beach Blvd, Revere, MA 02151, United States

September 13, 2020 12:00 PM

“One employee at Kelly's Roast Beef located on Revere Beach Blvd in Revere tested positive for COVID-19.

Source: wcvb.com See Less
Reported By SafelyHQ.com User

September 13, 2020 12:00 PM

“One employee at The Beef Restaurant & Pub on Leroy Street in Binghamton tested positive for COVID-19.

Source: wbng.com See Less
Reported By SafelyHQ.com User

September 2, 2020 8:00 PM

“Company name: Sunshine Mills, Inc.
Brand name: Family Pet, Heartland Farms, Paws Happy Life
Product recalled: Dog Food
Reason of the recall: Elevated levels of aflatoxin
FDA Recall date: September 02, 2020
Recall details: Sunshine Mills, Inc. is issuing a voluntary recall of certain dog food pr... See Moreoducts due to levels of Aflatoxin that are potentially above the acceptable limit.  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. The potential for aflatoxin levels above the acceptable limit in these products was discovered by routine sampling performed by the Louisiana Department of Agriculture and Forestry showing that a sample of a single 4-pound bag of one lot of the product contained elevated levels of aflatoxin. 

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. While no adverse health effects related to these products have been reported, Sunshine Mills, Inc. has chosen to issue a voluntary recall of these products as a precautionary measure in furtherance of its commitment to the safety and quality of its products. 

Pets that have consumed any of the recalled products and exhibit symptoms of illness including sluggishness or lethargy combined with a reluctance to eat, vomiting, yellowish tint to the eyes or gums, or diarrhea should be seen by a veterinarian. The affected products were distributed in retail stores nationally.  Retailers who received the recalled lots have been contacted and asked to pull these lots from their inventory and shelves. 

There are no other Family Pet®, Heartland Farms®, or Paws Happy Life® products or other lot codes of these products affected by this precautionary recall. 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. This is a voluntary recall being conducted in cooperation with the U.S. Food and Drug Administration. Products affected by this announcement:

+ Family Pet® Meaty Cuts Beef Chicken & Cheese Flavors Premium Dog Food.
- UPC: 3225120694. Size: 4 Lb. Lot codes: TD3 4/April/2020 | TD1 5/April/2020.
- UPC: 3225118078. Size: 14 Lb. Lot codes: TB1 4/April/2020 | TB2 4/April/2020 | TB3 3/April/2020
- UPC: 3225120694. Size: 28 Lb. TB3 3/April/2020
+ Heartland Farms® Grilled Favorites. Beef Chicken & Cheese Flavor.
- UPC: 7015514299. Size: 14 Lb. Lot codes: TB1 4/April/2020 | TB2 4/April/2020
- UPC: 7015514301 Size: 31 Lb. Lot codes: TA2 4/April/2020 | TA3 4/April/2020
+ Paws Happy Life® Butcher’s Choice Dog Food
- UPC: 3680035763. Size: 16 Lb. Lot codes: TA1 4/April/2020 | TA2 4/April/2020

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

July 13, 2020 11:30 PM

“The FSA announced the recall of various brands of raw dog food products containing beef by Benyfit Natural Pet Food because of the potential to be contaminated with Salmonella.

FSA advises pet owners if they have bought any of the recalled products not to use them. Instead, return them to the pla... See Morece of purchase for a full refund. These products have been sold by various independent pet food stores and online.

- Benyfit Natural 80-10-10 Beef Meat Feast (1kg) [Batch code. Best Before]
046-076. 16 March 2021 / 046-083. 23 March 2021 / 046-093. 2 April 2021 / 046-100. 9 April 2021

- Benyfit Natural 80-10-10 Beef Meat Feast (500g) [Batch code. Best Before]
47-076. 16 March 2021 / 47-083. 23 March 2021 / 47-093. 2 April 2021 / 47-100. 9 April 2021

- Unique Raw Duck, Beef & Ox Recipe (1kg) [Batch code. Best Before]
710-077. 17 March 2021 / 710-099. 8 April 2021

- Benyfit Natural Beef & Tripe (1kg) [Batch code. Best Before]
13-077. 17 March 2021 / 13-085. 25 March 2021 / 13-093. 2 April 2021 / 13-100. 9 April 2021

- Benyfit Natural Beef & Tripe (500g) [Batch code. Best Before]
14-077. 17 March 2021 / 14-086. 25 March 2021 / 14-093. 2 April 2021 / 14-100. 9 April 2021

- Benyfit Natural Succulent Beef (1kg) [Batch code. Best Before]
10-083. 23 March 2021 / 10-087. 27 March 2021 / 10-090. 30 March 2021 / 10-100. 9 April 2021

- Benyfit Natural Succulent Beef (500g) [Batch code. Best Before]
11-083. 23 March 2021 / 11-090. 30 March 2021 / 11-100. 9 April 2021

- Embark on Raw Natural Working Dog Food Beef Complete (454g) [Batch code. Best Before]
203-078. 18 March 2021 / 203-090. 30 March 2021 / 203-097. 6 April 2021

- Neew Dog Premium Beef (1kg) [Batch code. Best Before]
405-079. 19 March 2021 / 405-090. 30 March 2021 / 405-099. 8 April 2021

- Neew Dog Premium Beef (500g) [Batch code. Best Before]
406-090. 30 March 2021 / 406-097. 6 April 2021

- Unique Raw Chicken, Beef & Ox Recipe (1kg) [Batch code. Best Before]
707-098. 7 April 2021

When handling and serving raw pet food it is always advised to clean utensils and feeding bowls thoroughly after use. Consumers should wash hands thoroughly after handling raw pet food, bowls, utensils or after contact with the feces of animals. Raw pet food should be stored separately from any food (especially ready to eat foods).

Check the full recall details on the FSA website food.gov.uk

Source: FSA
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Reported By SafelyHQ.com User

June 5, 2020 7:57 PM

“I bought some beef jerky from there and it's definitely not good and it's got a weird powdery substance in it. I returned it and looked at the rest of their stock on the same item. The rest looked fine See Less
Reported By SafelyHQ.com User

June 4, 2020 12:00 PM

“Another 224 workers at Tyson's beef and pork processing plant in Council Bluffs have tested positive for the coronavirus

Source: desmoinesregister.com See Less
Reported By SafelyHQ.com User

Recent Interesting Reports

September 23, 2020 3:00 PM

“Company name: Sun Pharmaceutical Industries
Brand name: Riomet ER
Product recalled: Metformin Hydrochloride for Extended-Release Oral Suspension
Reason of the recall: Due to the Detection of N-Nitrosodimethylamine (NDMA) Impurity
FDA Recall date: September 23, 2020
Recall details: Sun Pharmace... See Moreutical Industries, Inc. (SUN PHARMA), a wholly owned subsidiary of Sun Pharmaceutical Industries Ltd. is voluntarily recalling one lot of RIOMET ER™ (metformin hydrochloride for extended-release oral suspension), 500 mg per 5 mL to the consumer level.  The reason for the recall is due to the level of N-Nitrosodimethylamine (NDMA), which has been found to be above the allowable Acceptable Daily Intake (ADI) limit established by the U.S. Food and Drug Administration. 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 and found in water and foods, including meats, dairy products, and vegetables.  To date, SUN PHARMA has not received any reports of adverse events related to this recall.  RIOMET ER™ (metformin hydrochloride for extended-release oral suspension) is a prescription oral medication indicated as an adjunct to diet and exercise to improve glycemic control in adults and pediatric patients 10 years of age and older with type 2 diabetes mellitus.  RIOMET ER™, when reconstituted, is packaged in a 16 oz. (473 mL) round bottle.  Each carton contains one bottle of drug pellets, one bottle of diluent, and one dosing cup.  The affected RIOMET ER™ is the following lot:

- RIOMET ER™ (metformin hydrochloride for extended-release oral suspension) 500 mg per 5 mL. Lot # AB06381. NDC #10631-019-17. Expiration Date: 10/2021. Number of Units: 747 cartons.

The product can be identified by the bottles or carton labeled as RIOMET ER™ (metformin hydrochloride for extended-release oral suspension), containing the specific Lot Number and Expiration Date referenced above or on the labeling below. The product was distributed nationwide to wholesale customers.

SUN PHARMA is notifying its distributors and customers through its third-party Recall Coordinator (Inmar Inc.), via FedEx standard overnight shipping and will arrange for return of all recalled products.

Distributors and retailers that have RIOMET ER™ (metformin hydrochloride for extended release oral suspension), which is being recalled, should stop distributing and return it to place of purchase or as directed in the recall notification.

Patients taking RIOMET ER™ (metformin hydrochloride for extended-release oral suspension), 500 mg per 5 mL are advised to continue taking their medication and contact their pharmacist, physician, or medical provider for advice regarding an alternative treatment. According to the U.S. Food & Drug Administration, it could be dangerous for patients with this serious condition to stop taking their metformin without first talking to their health care professionals. Please visit the agency’s website for more information at fda.gov

Consumers with questions regarding this recall can contact SUN PHARMA by calling 1-800-818-4555 Monday through Friday between 8:00 am to 5:00 pm EST or e-mailing drug.safetyUSA@sunpharma.com. 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

September 11, 2020 4:00 PM

“Company name: Goodie Girl Tribeca LLC
Brand name: Goodie Girl
Product recalled: Goodie Girl GF Magical Animal Crackers
Reason of the recall: May Contain Undeclared Wheat
FDA Recall date: September 11, 2020
Recall details: Goodie Girl Tribeca LLC announced today it is voluntarily recalling 389... See Morecases of a single date code of 7 oz. Goodie Girl Magical Animal Crackers, with a “best by” date of Jan 11, 21A3, after learning that the product may contain undeclared wheat ingredients. People who have an allergy or severe sensitivity to wheat run the risk of allergic reaction if they consume the product contained in the recalled boxes. There has been an individual with a wheat allergy that was treated for a wheat allergen reaction.

This recall affects only 389 cases of the following product, which were distributed in retail stores nationwide:
- Description; Goodie Girl GF Magical Animal Crackers
UPC# 8-5598700395-3
Size; 7 Ounces
Best By Date; Jan 11, 2021
Distributed between 4/17/2020 – 5/7/2020

This recall does not apply to any other “best by” dates, sizes or varieties of Goodie Girl Tribeca LLC. This recall was initiated in cooperation with the FDA and the third-party co-packer that produced the product. Product with this particular “best by” date was shipped and distributed by Goodie Girl Tribeca to its customers' warehouses located in Virginia, Pennsylvania, Georgia, New Hampshire, California. Consumers seeking a refund or additional information may contact info@goodiegirl.com or call 201-941-2000 9am – 5pm est.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

September 10, 2020 9:00 PM

“Company name: Pretty Thai
Brand name: Pretty Thai
Product recalled: Pretty Thai Sweat Chili Sauce
Reason of the recall: May contain Pretty Thai Peanut Sauce
FDA Recall date: September 10, 2020
Recall details: Company Announcement Pretty Thai of Austin, Texas, is recalling Pretty Thai Peanut Sau... See Morece that may have been mislabeled as Pretty Thai Sweet Chili Sauce. There is a risk that a person with an allergy or severe sensitivity to peanuts could unintentionally consume a product containing peanuts because of this error. No illnesses have been reported to date.

The product was distributed to H-E-B and Central Market stores in Texas from March 19, 2020 to September 8, 2020. The product is packaged in clear, cylindrical PET bottles with black flip-top caps and clear labels with white print. The recall is for Pretty Thai Peanut Sauce with the Lot Code 0772000123. A small number of the Pretty Thai Peanut Sauce bottles were discovered to have been mislabeled as Pretty Thai Sweet Chili Sauce. Pretty Thai Peanut Sauce is yellow or gold in color, while Pretty Thai Sweet Chili Sauce is dark red in color. People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume the mislabeled product.

Pretty Thai and its manufacturer, Ponder Foods, have coordinated efforts with H-E-B to remove all of the affected product from the shelves and from distribution. Out of an abundance of caution, we are alerting consumers in Texas who may have purchased either Pretty Thai Peanut Sauce or Pretty Thai Sweet Chili Sauce to check any product for Lot Code 0772000123. For consumers with no peanut allergy, this Lot Code of Pretty Thai Peanut Sauce, as well as any Lot Code of Pretty Thai Sweet Chili Sauce are completely safe to consume. Product may be returned to H-E-B and/or Central Market for a full refund. Subsequent investigation indicates the problem was caused by a temporary breakdown in the manufacturer's production and packaging processes.

Consumers with questions may contact the Pretty Thai brand directly via email at info@ptfawg.com or via telephone at 512 981 6170. Consumers or retailers may also contact the manufacturer, Ponder Foods, via email at info@ponder-foods.com or via telephone at 469 914 0052 (M-F, 9:00am-5:00pm CDT). Attached below is a photo of the mislabeled product with the affected Lot Code.  

Check the full recall details on fda.gov

Source: FDA
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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 14, 2020 10:41 AM

“I was do discussed I took one bite of my cheeseburger There was a long black curly hair wrapped into all around the burger it wasn't just a little piece of hair it was long and curly very bad turned me off from eating there now and I ate there lots it was on 09/05/2020 @ 2:46pm I took it back to the... See Morem rite away. I haven't posted the picture .. yet but feel like I should People shouldn't have to check and look at ther food especially from a place like this should n able to trust that ther nothing in there that shouldn't b why are they not wearing hair nets!? I watched the girls making the food in the back no one is wearing hair nets See Less
Reported By SafelyHQ.com User

September 3, 2020 7:00 PM

“Company name: AJR Trading LLC
Brand name: bio aaa
Product recalled: Hand Sanitizer
Reason of the recall: Possible presence of methanol
FDA Recall date: September 03, 2020
Recall details: AJR Trading is voluntarily recalling 2,004 units of lot 20DF8307 of bio aaa Advance Hand Sanitizer currentl... See Morey in US distribution, packaged in 480 mL bottles, to the consumer level. This lot of bio aaa Advance Hand Sanitizer has been tested and meets all appropriate specifications and tests. However, in an abundance of caution, these units are being recalled because of possible presence of methanol in other lots of bio aaa Advance Hand Sanitizer.

Risk Statement: Substantial methanol exposure could 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 may be at risk; young children who accidently ingest them and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning.

To date, AJR Trading has not received reports of adverse events related to this recall.

The product is used as a hand sanitizer to reduce bacteria when soap and water is not available and is packaged in 480 mL plastic bottles UPC 7502272121085.  AJR Trading is recalling lot 20DF8307, expiration date April 2022. The product can be identified by the images below. Product was distributed in Miami beginning in April 2020. AJR Trading is notifying its customers by phone calls, e-mails, and letters.  AJR Trading is arranging for refund and destruction of recalled products.

Consumers/distributors/retailers that have the above listed lots of bio aaa Hand Sanitizer, which is being recalled, should stop using or distributing the products immediately and mail the products to AJR Trading at the following address for refund: 814 Ponce de Leon Blvd, suite 218. Coral Gables, FL. 33134. Consumers with questions regarding this recall can contact AJR Trading by phone insert 305-302-8416 or e-mail to ajrtrading15@gmaill.com Monday to Friday from 10:00 am to 5:00 pm Central Time.

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. 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. Complete and submit the report Online

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Check the full recall details on fda.gov

Source: FDA
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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

Insects in Food, Italist Pizza Pasta Bar, проспект Соборності, Kyiv, Ukraine

Italist Pizza Pasta Bar, проспект Соборності, Kyiv, Ukraine

September 5, 2020 12:03 PM

“Midgets in restaurant flying over my food, disgusting, waiter said it’s “nature” See Less
Reported By SafelyHQ.com User

September 4, 2020 7:00 AM

“Company name: RLC Labs, Inc
Brand name: RLC Labs
Product recalled: Nature-Throid® and WP Thyroid®
Reason of the recall: Product may be sub potent
FDA Recall date: September 02, 2020
Recall details: RLC Labs, Inc. is voluntarily recalling a total of 483 lots of Nature-Throid® and WP Thyroid® in... See Moreall strengths, all counts of product within current expiry to the consumer level. The products are being recalled because testing of samples from  six (6) lots  by the U.S. Food and Drug Administration found the samples to be sub potent. The product may have as low as 87% of the labeled amount of Liothyronine (T3) or Levothyroxine(T4).

Risk Statement: Patients being treated for hypothyroidism (underactive thyroid), who receive sub potent Nature-Throid® or WP Thyroid®, may experience signs and symptoms of hypothyroidism (underactive thyroid) which may include, fatigue, increased sensitivity to cold, constipation, dry skin, puffy face, hair loss, slow heart rate, depression, swelling of the thyroid gland and/or unexplained weight gain or difficulty losing weight. There is reasonable risk of serious injury in newborn infants or pregnant women with hypothyroidism including early miscarriage, fetal hyperthyroidism, and/or impairments to fetal neural and skeletal development. In elderly patients and patients with underlying cardiac disease toxic cardiac manifestations of hyperthyroidism may occur, such as cardiac pain, palpitations or cardiac arrhythmia.

RLC Labs, Inc. has not received any reports of adverse events related to this recall. Nature-Throid® and WP Thyroid® (thyroid tablets, USP) is composed of liothyronine and levothyroxine, and are used to treat hypothyroidism (underactive thyroid). The products subject to recall are packaged in 30, 60, 90, 100 and 1,000 count bottles. To best identify the product, the NDC’s, Product Descriptions, Lot Numbers and Expiration Dates are listed in the link below.

These lots were distributed nationwide in the USA to RLC Labs, Inc.’s direct accounts, including healthcare professionals and retail pharmacies. RLC Labs, Inc. is proactively notifying its wholesalers by email, mail and phone to discontinue distribution of the product being recalled and is arranging for the return of all recalled products. Patients who are currently taking Nature-Throid® and WP Thyroid® should not discontinue use without contacting their healthcare provider for further guidance and/or replacement prescription.

Consumers with questions about the recall can email RLC Labs, Inc. at recall@rlclabs.com or contact RLC Labs, Inc. Customer Service at 1-877-797-7997, Monday through Thursday from 7:00 am to 4:00 pm MST (AZ) and Friday from 7:00 am to 3:00 pm MST (AZ). 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. 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. Complete and submit the report Online.

Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

September 5, 2020 12:01 PM

“Company name: CorgioMed LLC
Brand name: Leafree
Product recalled: Hand sanitizer
Reason of the recall: Product is labeled as edible alcohol.
FDA Recall date: September 03, 2020
Recall details: CorgioMed, LLC is voluntarily recalling all lots of Leafree Instant Hand Sanitizer-Aloe Vera, within e... See Morexpiry to the consumer level.  The products are being recalled because they are labeled as “EDIBLE ALCOHOL”. Leafree Hand Sanitizer is an alcohol-based hand rub to be applied externally to reduce bacteria on the skin when soap and water are not available.

Risk Statement: Ingesting hand sanitizer, which is intended for topical use, may 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. Young children may experience a sharp decrease in blood sugar which may result in death. Pregnant women who ingest alcohol have experienced birth defects and developmental disabilities. Nursing mothers who ingest alcohol in above moderate levels may see developmental, growth and sleep pattern damages in their babies and may experience impaired judgement and ability to safely care for their child.

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.  The labeling of this product as ‘edible alcohol’ may promote this behavior. The product is used as a hand sanitizer and is packaged in 100 ml (UPC #6970495860325), 300 ml (UPC #69705860318) and 500 ml (UPC #6970495860301) bottles. 

Product was distributed Nationwide via CorgioMed website. CorgioMed LLC is notifying its distributors and customers by email and is arranging for return or disposal of all recalled products. Distributors and Consumers with questions regarding this recall can contact CorgioMed LLC by emailing to: contact@corgiomed.comor phone: 301-978-3898 from September 1st to September 30th, 2020. 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. 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. Complete and submit the report Online.

Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Check the full recall details on fda.gov

Source: FDA
See Less
Reported By SafelyHQ.com User