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Cash Saver Food Outlet, Fleur Drive, Des Moines, IA, USA
Total all time reports: 1
Latest report: June 15, 2020 2:43 PM
Bone fragment in Carl Budding meat packets
June 15, 2020 2:43 PM
“Bone fragment in Carl Budding meat packets. Mixed chicken and ... om/product/honey#scroll" title="Product: Honey">honey ham so not sure which one. ”
Wing Zone, 1694 Montgomery Hwy, Hoover, AL 35216, United States, Wing Zone, 1694 Montgomery Hwy, Hoover, AL 35216, United States
Wing Zone, 1694 Montgomery Hwy, Hoover, AL 35216, United States
July 10, 2020 5:30 AM
“since no one wants to answer me when I ask about being served raw chicken I’ll just keep trying. Feel free to actually reach out ”
Fireworks everynight. Police are not doing anything, Gantry Plaza State Park, 47th Road, New York, NY, USA
Gantry Plaza State Park, 47th Road, New York, NY, USA
July 8, 2020 8:36 AM
“Fireworks are going off every night between midnight and 5 am. Multiple reports to 311 and the police have done nothing. They are onsite and have done nothing. The building is planning a community watch initiative. ”
Viva Chicken Elizabeth Avenue, 1617 Elizabeth Ave, Charlotte, NC 28204, United States, Viva Chicken Elizabeth Avenue, 1617 Elizabeth Ave, Charlotte, NC 28204, United States
Viva Chicken Elizabeth Avenue, 1617 Elizabeth Ave, Charlotte, NC 28204, United States
July 7, 2020 4:35 PM
“you guys sold me undercooked chicken ”
Hunters Point, Queens, NY, USA
June 25, 2020 9:40 AM
“people were lighting fireworks off about every hour starting at midnight. fireworks have gone off nightly for about a week, but last night was the worst. The cops are not stopping it. ”
Jacksonville, FL, USA
June 22, 2020 11:09 AM
“While eating a Nature Valley Sweet & Salty nut chewy granola bar I taste vomit in it. I have been eating these bars for years and I have never tasted vomit in them unlike today. ”
Smoky Boys Stevenage, Wedgwood Way, Pin Green, Stevenage, UK, Smoky Boys Stevenage, Wedgwood Way, Pin Green, Stevenage, UK
Smoky Boys Stevenage, Wedgwood Way, Pin Green, Stevenage, UK
May 26, 2020 3:36 AM
“I would like to report a bad restaurant as they delivered a half raw chicken to me and did not even bother to solve it with me.
Please look at the picture. Clearly to see the half raw thing! Dangero ... us! ”
Fresh Thyme Farmers Market, Golden Gate Plaza, Mayfield Heights, OH, USA
May 4, 2020 1:46 PM
“I went to buy GT’s Cocoyo and more than half of the yogurt they had was expired by more than 7 days. Yikes ”
I was thrown out of a Ralph's market for being 58 and a senior by manager, Ralphs, North Sepulveda Boulevard, El Segundo, CA, USA
Ralphs, North Sepulveda Boulevard, El Segundo, CA, USA
April 4, 2020 11:43 PM
“Store sales rep for Ralph's at 15 minutes to close as I was walking out approached me before 10 pm and accused me of going in and out a couple of times and not buying anything ..also while using the toilet ...during the virus lockdown female yanks on bathroom door yelling I have to clean I have to c ... lean.. trying to rip handle off...I said I'm on the pot sorry...so my reply to sales rep is I'm a customer of Ralph's and a senior. I was thrown out of a Ralph's market for being 58 and a senior by manager and store manager a couple days ago and sent a letter barring me from all Ralph's regardless that I at 8:30 am should have gone to the head of the line and that I was with my 83 year old mother waiting in the car as usual every morning...and also refused me going to bathroom had to go really bad.. ”
March 20, 2020 2:30 AM
“since last night i have mild fever and a soar throat. these are symptoms of coronavirus. i am in london and can not be tested as my situation is not urgent. hope it stays this way. per advice of NH will be self-isolating. i am OK and have food and water for seven days. ? ”
Two employees test positive for Covid-19, Rita's Cantina, 401 SE 5th St, Des Moines, IA 50309, United States
Rita's Cantina, 401 SE 5th St, Des Moines, IA 50309, United States
July 6, 2020 12:00 PM
“Two employees tested positive for COVID-19
at Rita's Cantina in Des Moines
Source: weareiowa.com ”
Recent Interesting Reports
KFC Walsall - Junction 10 M6 Services, Walsall, Wolverhampton WS2 8RL, United Kingdom, KFC Walsall - Junction 10 M6 Services, Walsall, Wolverhampton WS2 8RL, United Kingdom
KFC Walsall - Junction 10 M6 Services, Walsall, Wolverhampton WS2 8RL, United Kingdom
May 27, 2020 9:34 AM
Wendy's, 6892 Garners Ferry Rd, Columbia, SC 29209, United States, Wendy's, 6892 Garners Ferry Rd, Columbia, SC 29209, United States
Wendy's, 6892 Garners Ferry Rd, Columbia, SC 29209, United States
June 25, 2020 5:31 PM
“serving raw chicken ”
Saniderm Advanced Hand Sanitizer, 70% alcohol content - recalled due to potential presence of methanol (wood alcohol), USA
June 29, 2020 2:01 PM
“Company name: UVT, INC.
Brand name: Saniderm
Product recalled: Advanced Hand Sanitizer, 70% alcohol content
Reason of the recall: Potential presence of methanol (wood alcohol)
FDA Recall date: June 29, 2020
Recall details: UVT, INC. is voluntarily recalling 38,830 liters of SANIDERM ADVANCED H ... AND SANITIZER, packaged in 1-liter bottles to the consumer level. The products are being recalled due to the potential presence of methanol (wood alcohol) To date, UVT, INC. has not received any reports of adverse events related to this recall.
The affected SANIDERM ADVANCED HAND SANITIZER includes lot number 0530, Expiration date 04/2022. The product can be identified by the label below. The product was distributed Nationwide in the United States. The product is used as a hand sanitizer and is packaged in 1-liter plastic bottles.
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.
UVT, INC. is notifying its distributors and customers by phone calls, emails and letter and is arranging for replacement and destruction of all recalled products. Consumers/distributors/retailers that have product which is being recalled should stop using products, initiate recalls to the user level, and return all products to the place of purchase.
Consumers with questions regarding this recall can contact UVT, INC. by phone (951) 427- 3108 or e-mail to firstname.lastname@example.org Monday to Friday from 9:00 am and 3:00 pm Pacific 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. 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 ”
Amneal Pharmaceuticals LLC Metformin Hydrochloride Extended-Release Tablets, USP 500mg and 750mg - recalled due to Due to detection of N-Nitrosodimethylamine (NDMA), USA
June 1, 2020 6:00 PM
“Company name: Amneal Pharmaceuticals LLC
Brand name: Amneal
Product recalled: Metformin Hydrochloride Extended-Release Tablets, USP 500mg and 750mg
Reason of the recall: Due to detection of N-Nitrosodimethylamine (NDMA)
FDA Recall date: June 01, 2020
Recall details: Amneal Pharmaceuticals L ... LC Bridgewater, New Jersey (Amneal), is voluntarily recalling all lots of Metformin Hydrochloride Extended-Release Tablets, USP, 500 mg and 750 mg, within expiry to the Retail Level. Amneal was notified by the U.S. FDA that the Agency’s testing of seven lots of Metformin Hydrochloride Extended-Release Tablets, USP, 500 mg and 750 mg, showed N-Nitrosodimethylamine (NDMA) amounts above acceptable FDA levels.
FDA recommended the recall of the seven tested lots. Amneal has agreed to this recall and has further decided to extend the recall to all lots within expiry of Metformin Hydrochloride Extended-Release Tablets, USP, 500 mg and 750 mg, out of an abundance of caution. Further scientific evaluations are ongoing at Amneal. To date, Amneal has not received any reports of adverse events that have been confirmed to be directly related to this recall. Amneal’s Metformin Hydrochloride Immediate Release Tablets, USP are not affected by this recall.
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. Metformin HCl Extended-Release Tablets, USP, 500 mg and 750 mg, manufactured by Amneal, are prescription, solid oral products that are indicated as an adjunct to diet and exercise to improve blood sugar control in adults with type 2 diabetes mellitus. The Metformin Hydrochloride Extended-Release Tablets, USP, 500 mg and 750 mg, subject to the recall, are identified by the NDC numbers stated on the product label.
Metformin HCl Extended-Release Tablets, USP, 500 mg
53746-178-01. 100 count bottles
53746-178-05. 500 count bottles
53746-178-10. 1000 count bottles
53746-178-90. 90 count bottles
53746-178-Bulk. Bulk Box
65162-178-09. 90 count bottles
65162-178-10. 100 count bottles
65162-178-11. 1000 count bottles
65162-178-50. 500 count bottles
Metformin HCl Extended-Release Tablets, USP, 750 mg
53746-179-01. 1000 count bottles
53746-179-Bulk. Bulk Box
65162-179-10. 100 count bottles
The affected Metformin Hydrochloride Extended-Release Tablets, USP, 500 mg and 750 mg, lots were distributed nationwide in the US directly to Wholesalers, Distributors, Retailers, and Repackagers.
Amneal is notifying its direct customers via mail (UPS Standard Overnight) by mailing a recall notification letter and is arranging for the return of all the recalled products. Anyone with an existing inventory of the product should quarantine the recalled lots immediately.
Check the full recall details on fda.gov
Source: FDA ”
Brooklyn, NY, USA
June 10, 2020 7:52 PM
“Peaceful Black Lives Matter protest through brooklyn on bikes ”
Gramercy Park, Manhattan, New York, NY, USA
March 25, 2020 8:31 PM
“Building management informed us that someone was confirmed tested positive in our building. ”
Infusion pumps and sets - recalled due to pumps may not deliver fluid at the accuracy specified in the instructions, USA
April 29, 2020 7:00 PM
“Company name: CME America
Brand name: CMEAmerica BodyGuard
Product recalled: Infusion pumps and infusion sets
Reason of the recall: pumps may not deliver fluid at the accuracy specified in the instructions for use and infusion sets may under-deliver fluids
FDA Recall date: April 29, 2020
Recall ... details: CME America, a wholly owned subsidiary of BD (Becton, Dickinson and Company), a leading global medical technology company, today issued the following update regarding two previously announced voluntary recalls, one related to all models of CMEAmerica BodyGuard® infusion pumps (FDA Recall Number: Z-1474-2020) and the other related to one of the device's infusion sets (FDA Recall Number: Z-1442-2020). Both previously announced recalls have now been designated as Class I recalls by the U.S. Food and Drug Administration (FDA), which means the FDA believes that there is a reasonable probability that use of the recalled product(s) will cause serious adverse health consequences or death.
CME America previously notified customers affected by each recall and provided guidance on the potential impact to device performance when the affected products were used. Today, the company has issued an updated customer letter with additional guidance and to inform customers of the decision to suspend distribution of the BodyGuard® infusion pump system and to remove all existing products from the U.S. market.
The following is a summary of each individual product recall details:
CMEAmerica BodyGuard® Infusion Pump Recall
Details On Jan. 6, 2020, the company initiated a voluntary recall to notify customers of certain scenarios where pumps may not deliver fluid at the accuracy specified in the instructions for use that could result in a slower than expected delivery of medication (under-infusion), and/or faster than expected delivery of medication (over-infusion). Results indicate that pumps may have a delivery inaccuracy of up to ~13%. To date, no reports of patient injury has been received related to this previously announced voluntary recall. CME America has assessed the potential risks associated with the issues outlined in the initial voluntary recall and determined that the BodyGuard® infusion pump may continue to be used in certain situations in accordance with the Operator's Manual and the additional mitigations outlined in the updated customer letter until the pumps have been removed from the market.
To ensure customers retain access to critical medical equipment, particularly as the COVID-19 pandemic continues to evolve in the United States, CME America will implement a phased market removal and will continue to support the following activities in order to help limit clinical disruption and maintain patient focus during the COVID-19 pandemic: Use of products in the field in accordance with the Operator's Manual and the additional mitigations outlined in the updated customer letter; Product service and repair activities at CME America and Authorized Service Depots; and Supply of infusion sets and accessories to support the infusion pumps remaining in the field.
The BodyGuard® infusion pump is designed to deliver fluids or medications into a patient's body in controlled amounts. The pump administers fluids through an infusion tubing set into a patient's vein or through other cleared routes of administration. The system is intended for patients who require maintenance medications, PCA therapy, parenteral nutritional fluids, and general IV fluid therapy in hospital and home care environments. Typical applications for the BodyGuard® infusion pumps include but are not limited to chemotherapy, pain management, TPN, enteral nutrition fluids and antibiotics.
The recall and market removal affect approximately 28,400 devices, including all models of BodyGuard® infusion pumps listed below. These devices are primarily used in outpatient settings.
- BodyGuard 121
- BodyGuard 323
- BodyGuard 545*
- BodyGuard 575*
- BodyGuard 545 ColorVision
- BodyGuard 575 ColorVision
*Note: These two pump models were inadvertently left out of the initial customer notification
CMEAmerica BodyGuard® Microset Infusion Set Recall
Details On Sept. 16, 2019, the company initiated a voluntary recall to notify customers that certain lots of BodyGuard® Microset infusion sets, when used with the BodyGuard® infusion pump, may under-deliver fluids up to 50% at the highest flow rates. At the time of the recall, CME America informed customers in the recall announcement to discard all remaining inventory of the infusion sets (Catalog #A120-003XYVA) and committed to reimbursing impacted customers. To date, no reports of patient injury has been received related to this previously announced voluntary recall. CME America immediately stopped shipments of the affected infusion sets. This FDA classification does not change the previous guidance provided in the company's September recall announcement to customers. Affected products include:
CMEAmerica BodyGuard® Microset, Catalog #A120-003XYVA.
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 ”
Wendy's, Orlando, FL 32827, United States
June 2, 2020 9:33 PM
“just received this at your MCO airport location.. i didn’t cut into this. i was served half a raw sandwich ? ”
McDonald's, North Reed Avenue, Reedley, CA, USA
April 17, 2020 11:57 PM
“I didn’t eat it but my Mcchicken had a black sliver in it and this was going to be eaten by my grandma and I went to have it replaced but they gave me the same ... felyhq.com/product/burger#scroll" title="Product: Burger">burger but took out the sliver after five people touching it too and tried to pass it off as a fresh burger and I have pictures of before and after but I don’t know how to attach pictures ”
Trader Joe’s Union Square Location Temporarily Closes After Staffer Test Positive for COVID-19, Trader Joe's, 142 E 14th St, New York, NY 10003, United States
Trader Joe's, 142 E 14th St, New York, NY 10003, United States
March 25, 2020 12:39 PM
“Trader Joe’s announced that the Union Square location of its grocery store had temporarily closed for cleaning, as had the adjoining wine store, the company’s only in the city.
The staffer who tested pos ... itive at the Union Square Trader Joe’s was last in the store on Sunday, March 22, the company said. According to the store’s online hours on Google Maps, the Trader Joe’s grocery and wine stores are expected to reopen Saturday.
Source: ny.eater.com ”