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Eighteen at the Radisson, West 5th Street, Covington, KY, USA
Total all time reports:
1
Latest report: March 12, 2020 8:47 PM
The Radisson in Covington Ky , had a roach crawl across the table today.
March 12, 2020 8:47 PM
“We set down and ordered our drinks and when the waiter set down the menus the roach crawled across the table See Less”
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Related Reports
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 See Less”
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Long black curly hair wrapped into my cheeseburger, McDonald's, 1219 Marine Dr, North Vancouver, BC V7P 1T3, Canada
McDonald's, 1219 Marine Dr, North Vancouver, BC V7P 1T3, Canada
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”
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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”
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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 See Less”
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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 See Less”
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September 1, 2020 4:36 PM
“Fresco Foods Inc. of Tampa, FL is voluntarily recalling ALL units of Ancient Grain Jackfruit Bowl sold at Publix because it may contain an undeclared allergen, FISH (anchovies). People who have an allergy or severe sensitivity to FISH (anchovies) run the risk of serious or life-threatening allergic... See Morereaction if they consume these products.
The allergy alert was initiated after it was discovered that the Ancient Grain Jackfruit Bowl containing Fish was distributed in packaging that did not reveal the presence of fish. Subsequent investigation indicates the problem was caused by sourcing the wrong sub-ingredient.
- Eat Fresco Ancient Grain Jackfruit Bowl. GTIN: 85898800510. Lot/Exp. Date: ALL
Individuals with an allergy or sensitivity to fish (anchovies) should not consume this product. Households that include individuals with an allergy or sensitivity to fish (anchovies) should dispose of the product or return it to the place of purchase for a refund.
Consumers with questions may contact Fresco Foods, Inc. at (813) 551-2100.
Check the full recall details on corporate.publix.com
Source: Publix See Less”
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Cheese slicer is not clean., Monmouth Beach Supermarket, Riverdale Avenue, Monmouth Beach, NJ, USA
Monmouth Beach Supermarket, Riverdale Avenue, Monmouth Beach, NJ, USA
August 24, 2020 1:28 PM
“I did not get ill because I threw the product away. But on Saturday 8/22 I ordered 1 lb of White American Boars Head cheese from MB market and when I came home my cheese had black streaks on it - it was clear that slicer had some residue on it when it was being used to slice my cheese. I hope it... See Morewas other food residue but given the color i feared it was metal residue from the machine. See Less”
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Unsanitary food worker and cold food., Piadina Italian Market Sandwich, El Camino Real, Tustin, CA, USA
Piadina Italian Market Sandwich, El Camino Real, Tustin, CA, USA
August 24, 2020 12:01 PM
“I have eaten here 10+ times but this time I picked up an order but the order wasn't ready when I arrived. They were still making the food. There was a guy with dark hair and a VERY LONG beard preparing food, around the food, etc without a hair guard/beard snood/no beard net. It was really gross!! I... See Morethink he might have been the manager? He told others when to go to break but he was all around the food. He (and his LONG beard) were hovering over the food prep. Maybe seeing that grossed me out, but when I ate the food (sandwiches) they were not hot/warm. It is a panini hot press sandwich. . .why was it practically cold? I don't think the food is being prepared properly and the beard guy needs to wrap it up! See Less”
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Undercooked Burger, Steak 'n Shake, Fayetteville Road, Garner, NC, USA
Steak 'n Shake, Fayetteville Road, Garner, NC, USA
July 30, 2020 11:37 AM
“I feel like I've been cordial enough. Unfortunately, their response hasn't been. They serves undercooked food. See Less”
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Raw Burger, McDonald's, 1198 South Hairston Road, Stone Mountain, GA 30088, USA
McDonald's, 1198 South Hairston Road, Stone Mountain, GA 30088, USA
July 22, 2020 11:40 AM
“Late night snack turned into late night disgusting food! The worst service I have ever received! RAW BURGER! The drink is NOT sweet tea. Check the receipt! I called the 24hr number no answer! See Less”
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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 See Less”
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Worms in my Banana Nut Muffins, Walmart Supercenter, Navarre Avenue, Oregon, OH, USA
Walmart Supercenter, Navarre Avenue, Oregon, OH, USA
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”
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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 See Less”
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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 See Less”
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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”
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2 people found this review helpful
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 See Less”
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COMERCIAL MEXICANA INNTERNATONAL INC ASSORTED FRUIT JELLY BAG & JELLY ANIMAL JAR - recalled due to Potential Choking Hazard, Forkston, PA, USA
Forkston, PA, USA
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 See Less”
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Cleaner Hand Sanitizer - recalled due to Potential Presence of Methanol (Wood Alcohol), United States
United States
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 See Less”
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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 See Less”
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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 See Less”
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