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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: Cheese

Updated: September 29, 2020 12:00 PM

September 29, 2020 12:00 PM

“Another employee(1) at SOUTHWEST CHEESE LLC in CLOVIS, NM tested positive for Covid-19. Event Date: 09/29/2020, RR-1632

Source: env.nm.govSee Less
Reported By SafelyHQ.com User

, Larchmont Village Wine, Spirits & Cheese, North Larchmont Boulevard, Los Angeles, CA, USA

Larchmont Village Wine, Spirits & Cheese, North Larchmont Boulevard, Los Angeles, CA, USA

September 22, 2020 12:00 PM

“An employee at Larchmont Village Wine and Cheese shop in Los Angeles tested positive for COVID-19. Larchmont Village Wine and Cheese shop closed the store Friday after the positive for COVID-19.

Source: larchmontbuzz.comSee Less
Reported By SafelyHQ.com User

Covid-19 OSHA Complaint, Walmart Supercenter, 1011 US Highway 72 East, Athens, Alabama 35611, USA

Walmart Supercenter, 1011 US Highway 72 East, Athens, Alabama 35611, USA

September 22, 2020 12:00 PM

“1. Employees who have tested positive and informed the employer have been told to keep quite or face termination.
2. Employees, exposed to a coworker that has tested positive for the COVID-19, are not being informed of contact or if they need to be tested.
3. Employees in the deli are exposed to a... See Moremputation injuries due to meat/cheese slicers in the deli turning on automatically.
4. Employees in the deli and/or meat department are exposed to slips and falls from ice accumulating in and around the freezer unit door.
5. Employers in the deli are exposed to burns due to a hose on a fryer with a broken handle.
6. Employees in the deli are exposed to burns due to a fryer that stops working, forcing the tub containing hot oil to be removed.


Source: Osha.gov | Receipt Date: 2020-07-15
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Reported By SafelyHQ.com User

September 23, 2020 9:00 AM

“Report date: Sep 17, 2020
2. City of chicago food service sanitation certificate
- comments: observed no valid city of chicago food sanitation certificate posted on the premises. Management instructed that a certified food manager must be present at all times while tcs foods are being prepared a... See Morend served. Priority foundation 7-38-012. Citation issued.

11. Food obtained from approved source
- comments: observed food stored in the walk-in cooler from an unapproved source. Observed 20 packages of cream kajmak spread manufactured from george's food stored in a plastic container inside of the walk-in cooler. No invoice was provided for the packaged food. A held for inspection tag was placed on the container of food. Management instructed not to sell this product. Priority 7-38-005. Citation issued.

37. Food properly labeled; original container
- comments: observed prepackaged foods such as cheeses, breads, and candies not labeled to indicate the name and address of the manufacturer, net contents, ingredients, or weight. Management instructed to label all prepackaged foods.

38. Insects, rodents, & animals not present
- comments: observed evidence of rodent activity on the premises. Observed approximately 100 mouse droppings on the floor and on the food storage shelves in the retail display area, rear storage rooms and in the utility room next to the 3 compartment sink. Management instructed to clean and remove all rodent droppings from all affected areas. Additional pest control service is needed to eliminate the pest activity. Priority foundation 7-38-020(a). Citation issued.

54. Garbage & refuse properly disposed; facilities maintained
- comments: observed garbage overflowing over the top of the garbage dumpsters so that the dumpster lids could not be closed. Management instructed to provide adequate garbage pickup so that the garbage does not overflow over the top of the garbage dumpsters. Also remove all old tires stored behind the dumpsters. Priority foundation 7-38-020(b). Citation issued.

55. Physical facilities installed, maintained & clean
- comments: clean the floor throughout the premises especially underneath the food storage shelves.

64. Public health nuisance
- comments: observed no social distancing by customers while waiting in line to check out at the register. Observed 6 customers standing in line less than 6 feet apart from each other. Management instructed to ensure that all customers practice social distancing while shopping inside of the store. Citation issued 7-28-060.

Source: chicago.gov
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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 21, 2020 12:00 PM

“Another employee(1) at SOUTHWEST CHEESE LLC in CLOVIS, NM tested positive for Covid-19. Event Date: 09/21/2020, RR-1294

Source: env.nm.govSee Less
Reported By SafelyHQ.com User

September 16, 2020 12:00 PM

“Another employee(1) at SOUTHWEST CHEESE LLC in CLOVIS, NM tested positive for Covid-19. Event Date: 09/16/2020, RR-1124

Source: env.nm.govSee Less
Reported By SafelyHQ.com User

September 15, 2020 12:00 PM

“Unknown number of employees at SOUTHWEST CHEESE CO LLC in CLOVIS, NM tested positive for Covid-19. Event Date: 09/14/2020, RR-0937

Source: env.nm.govSee Less
Reported By SafelyHQ.com User

September 16, 2020 9:00 AM

“Report date: Sep 14, 2020
22. Proper cold holding temperatures
- comments: observed improper cold holding temperature of tcs foods. Observed the following foods at improper temperatures inside of the walk-in cooler: eggs at 464. F, chicken at 47. 7f, tofu at 44. 6f, cream cheese at 47. 5f, and... See Morehalf and half creamer at 48. 2f. Management voluntarily discarded approximately 100# of food worth $800. Priority 7-38-005. Citation issued.

33. Proper cooling methods used; adequate equipment for temperature control
- comments: observed the walk-in cooler with an air temperature of 49. 5f. The cooler was used to store tcs foods such as eggs and cream cheese. Management instructed to repair and maintain the cooler below 41f. Priority 7-38-005. Citation issued.

38. Insects, rodents, & animals not present
- comments: observed 4 live cockroaches on the wall and floor of the food prep area and in the basement. Also observed 5 live small flies on the wall of the food prep area and outside of the washrooms. Additional pest control service is needed to eliminate the pest activity. Priority foundation 7-38-020(a). Citation issued.

38. Insects, rodents, & animals not present
- comments: clean the dead insects inside of the stove and on the floor in the basement.

49. Non-food/food contact surfaces clean
- comments: detail clean the grease on the interior bottom of the stove and gas lines behind the cooking equipment. Clean the food debris on the door handles and inside the prep coolers and freezers.

53. Toilet facilities: properly constructed, supplied, & cleaned
- comments: observed no covered waste receptacle inside of the employee washroom. Management instructed to provide.

55. Physical facilities installed, maintained & clean
- comments: detail clean the dust, food debris and grease on the walls and ceiling of the rear food prep area. Clean the floor throughout the rear prep area and basement.

56. Adequate ventilation & lighting; designated areas used
- comments: clean the heavy grease buildup on the ventilation hood and filters above the cooking equipment.

Source: chicago.gov
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Reported By SafelyHQ.com User

September 15, 2020 12:20 PM

“Ordered cheeseburger on lunch break, was eating it on my way back to work and it has shards of sharp, broken plastic pieces in itSee 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 10, 2020 5:00 PM

“Company name: Medek, LLC
Brand name: M
Product recalled: M Hand Sanitizer Alcohol Antiseptic 80%
Reason of the recall: Contains Methanol and may be Sub-Potent for Ethanol
FDA Recall date: September 10, 2020
Recall details: Medek, LLC is voluntarily recalling all lots of M Hand Sanitizer Alcoh... See Moreol Antiseptic 80% 128 oz/3,785 mL to the consumer level. FDA analysis found the M Hand Sanitizer to contain methanol and be sub-potent for ethanol.

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. In addition, the use of sub-potent hand sanitizer products can have adverse health consequences related to lack of efficacy and increased risk of infections. To date, Medek, LLC. has not received any reports of adverse.

The recalled product is used as a hand sanitizer for hand washing to decrease bacteria on the skin when soap and water are not available. The recalled Hand Sanitizer is packaged in a one (1) gallon (128 oz/3,785 mL) High-density polyethylene (HDPE) plastic bottle, NDC 75432-001-02. The recalled Hand Sanitizer was distributed directly to walk-in customers in Alamo, TX, between the dates of 04/17/2020 to 05/22/2020.

Medek, LLC is notifying its customers/distributors by recall letter and consumers via this press release. We are also notifying our distributors, who will help notify their customers by phone calls, emails, and/or mailed letters and is arranging for return of all recalled Hand Sanitizer. Consumers, distributors, and retailers that have recalled products should stop use or distribution and return to place of purchase. Consumers with questions regarding this recall can contact Medek, LLC at (956) 800-4366 (Monday to Friday from 9 am to 5 pm CST).

Consumers should contact their physician or healthcare provider if they experience any problem that may be related to the use of this 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 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

September 1, 2020 4:38 PM

“The FSIS announced the recall of approximately 1,202 pounds of ready-to-eat (RTE) chicken salad product by Ukrop’s Homestyle Foods due to misbranding and an undeclared allergen. The product may contain almonds, a known allergen, which are not declared on the product label.

The RTE chicken salad i... See Moretem was produced on August 26, 2020. The following product is subject to recall:

- 15-oz. round plastic containers containing “Ukrop’s Chicken Salad” with a sell by date of “09/02/20”.

The product subject to recall bears establishment number “P-19979” inside the USDA mark of inspection. These items were shipped to retail locations in North Carolina, Ohio, Virginia, and West Virginia. The problem was discovered after the firm received a consumer complaint reporting that the product contained almonds.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.

FSIS is concerned that some product may be in retailer and consumers’ refrigerators. Retailers who have obtained these products are urged not to sell them. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify that recalling firms are notifying their customers of the recall and that actions are being taken to make certain that the product is no longer available to consumers. Consumers and members of the media with questions about the recall can contact Susan Rowe, Executive Administrator, Ukrop’s Homestyle Foods, at (804) 340-3050.

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

Source: FSIS
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Reported By SafelyHQ.com User

September 17, 2020 11:00 PM

“Company name: Acella Pharmaceuticals, LLC
Brand name: NP Thyroid 15 & NP Thyroid120
Product recalled: Thyroid Tablets
Reason of the recall: Sub Potency
FDA Recall date: September 17, 2020
Recall details: Acella Pharmaceuticals, LLC is voluntarily recalling one lot of 15-mg and one lot of 120-mg... See MoreNP Thyroid®, Thyroid Tablets, USP [levothyroxine (T4) and liothyronine (T3)] to the consumer level. The products are being recalled because testing has found these lots to be sub potent. The product may have as low as 87% of the labeled amount of levothyroxine (T4). More information can be found at www.npthyroid.com/product-updates.

Risk Statement: Patients being treated for hypothyroidism (underactive thyroid), who receive sub potent NP 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.

To date, Acella has received four reports of adverse events for these lot numbers possibly related to this recall. NP Thyroid®, Thyroid Tablets, USP is composed of levothyroxine and liothyronine, and used to treat hypothyroidism (underactive thyroid). The products subject to recall are packed in 100-count bottles. See product images. To best identify the product, the NDC’s, Product Description, Lot Numbers and Expiration Dates are listed. These lots were distributed nationwide in the USA to Acella’s direct accounts, including wholesalers, pharmacies, and healthcare offices. Additionally, consumers may be able to determine that their product is not impacted by the recall if the “use by,” “discard after,” or “expiration date” on their prescription bottle is on or after December 2020.

Product NDC Lot # Exp. Date
NP Thyroid® 15, Thyroid Tablets, USP, ¼ grain (15 mg) 42192-327-01 M327E19-1 October 2020
NP Thyroid® 120, Thyroid Tablets, USP, 2 grain (120 mg) 42192-328-01 M328F19-3 November 2020

Acella is proactively notifying its wholesalers by email and phone to discontinue distribution of the two above referenced lots being recalled and is arranging for return of all recalled products. Patients who are currently taking NP Thyroid® from the lots being recalled should not discontinue use without contacting their healthcare provider for further guidance and/or a replacement prescription.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

September 2, 2020 11:41 PM

“The FSA announced the recall of Lamb and Carrot Dumplings by Freshasia Foods because they contain crustaceans, which are not mentioned on the label. This means the product is a possible health risk for anyone with an allergy to crustaceans.

FSA advises consumers not to eat the recalled product. I... See Morenstead, return it to the store from where it was bought for a full refund.

+ Freshasia Lamb and Carrot Dumplings. 400g. Batch code: 200402. Best before: 6 April 2021

Freshasia Foods is recalling the above product from customers and has been advised to contact the relevant allergy support organisations, which will tell their members about the recall. The company has also issued a point-of-sale notice to its customers. These notices explain to customers why the product is being recalled and tell them what to do if they have bought the product.

Check the full recall details on food.gov.uk

Source: FSA
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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
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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 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 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 netsSee Less
Reported By SafelyHQ.com User