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Updated: July 1, 2020 12:00 PM
burger-chan, Houston, TX 77046, USA
July 1, 2020 12:00 PM
“An employee at Burger-Chan in The Greenway Plaza tested positive for coronavirus.
Source: preview.houstonchronicle.com ”
Daddy's Burgers, 3422 Allen Pkwy, Houston, TX 77019, USA
June 22, 2020 12:00 PM
“An employee at Daddy’s Burgers, a burger pop-up at the Dunlavy on Allen Pkwy in Houston has tested posit ... ive for COVID-19.
Source: houston.eater.com ”
Hardee's, 2450 E Layton Ave, St Francis, WI 53235, United States, Hardee's, 2450 E Layton Ave, St Francis, WI 53235, United States
Hardee's, 2450 E Layton Ave, St Francis, WI 53235, United States
June 15, 2020 10:35 PM
“My sister got a raw burger today, and was given a "free meal coupon" when she called to complain. You think she wants to go back? This was inedible. She didn't finish it, so I don't know if it would hav ... e made her sick. ”
Whataburger, State Hwy 123, San Marcos, TX 78666, USA
June 14, 2020 12:00 PM
“An employee at Whataburger #178, 1004 State Hwy 123 has been reported positive for Covid-19
Source: ksat.com ”
Employee test positive for COVID-19, Nation's Giant Hamburgers, 3530 Truxel Rd, Sacramento, CA 95834, USA
Nation's Giant Hamburgers, 3530 Truxel Rd, Sacramento, CA 95834, USA
June 11, 2020 12:00 PM
“A Nation’s Giant Hamburgers employee in Sacramento has tested positive for COVID-19 a couple of weeks after its grand opening. The last time the employee worked at the restaurant was one week ago. ... Source: kcra.com ”
Two restaurant employees test positive for COVID-9, Shaggy's Burgers and Tacos, 1267 Enterprise Way, Huntsville, AL 35806, USA
Shaggy's Burgers and Tacos, 1267 Enterprise Way, Huntsville, AL 35806, USA
June 4, 2020 12:00 PM
“Two Shaggy’s Burgers and Tacos employees in Huntsville have tested positive for COVID-19. It is unknown when ... the customers worked last. If you visited the restaurant recently, please report it and any other location that you visited.
Source: whnt.com ”
Hardee's, Army Post Road, Des Moines, IA, USA
June 5, 2020 8:07 AM
Del Taco, Hamilton Road, Columbus, GA, USA
May 27, 2020 9:34 AM
“I contacted the manager at your store because my sister consumed an undercooked burger last night and is now very sick. He said that there was no way she can get sick from ... s://safelyhq.com/product/beef#scroll" title="Product: Beef">beef even though a quick google search says otherwise. I’m very disappointed. ”
Whataburger employee tests positive for COVID-19, Whataburger, 123 Creekside Crossing, New Braunfels, TX 78130, USA
Whataburger, 123 Creekside Crossing, New Braunfels, TX 78130, USA
May 24, 2020 12:00 PM
“A Whataburger had to shut down after the store reported one of its employees tested positive for COVID-19. If you visited the restaurant recently, please report it and any other location that you visited.
Source: news4sanantonio.com ”
Restaurant employee tests positive for COVID-19, Burger King, 823 E University Ave, Las Cruces, NM 88001, USA
Burger King, 823 E University Ave, Las Cruces, NM 88001, USA
May 17, 2020 12:00 PM
“A Burger King employee at the University Avenue location has tested positive for COVID-19. It is unknown when the employee last worked, but if you visited location recently, please report it and any oth ... er location that you visited.
Source: lcsun-news.com ”
Recent Interesting Reports
Madison Square Park, Madison Avenue, New York, NY, USA
June 5, 2020 4:54 PM
“Right now large protest march ”
Metformin Hydrochloride Extended-Release Tablets, USP 500mg - recalled due to Due to detection of N-Nitrosodimethylamine (NDMA), USA
June 5, 2020 5:00 PM
“Company name: Marksans Pharma Limited, India
Brand name: Time-Cap Labs, Inc.
Product recalled: Metformin Hydrochloride Extended-Release Tablets, USP 500mg
Reason of the recall: Due to detection of N-Nitrosodimethylamine (NDMA)
FDA Recall date: June 05, 2020
Recall details: Marksans Pharma Limi ... ted, India is voluntarily recalling Metformin Hydrochloride Extended-Release Tablets, USP 500mg, lot # XP9004, to the consumer level. FDA analysis has found the product to contain N-Nitrosodimethylamine (NDMA) levels in excess of the Acceptable Daily Intake Limit (ADI) of 96ng/day. 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 related to this recall to date. Metformin Hydrochloride Extended-Release Tablets, USP 500mg is indicated as an adjunct to diet and exercise to improve blood glucose control in adults with type 2 diabetes mellitus and is packaged in 100 count bottles with NDC code 49483-623-01. 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.
Product name: Metformin Hydrochloride Extended Release Tablets USP, 500 mg
Lot #: XP9004
Expiry Date (MM/YYYY): 12/2020
The product can be identified by lot # XP9004 and expiration date 12/2020. Metformin Hydrochloride Extended-Release Tablets, USP 500mg, lot # XP9004 was distributed by Time-Cap Labs, Inc. 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 lot.
Distributors/retailers that have Metformin Hydrochloride Extended-Release Tablets, USP 500mg, lot # XP9004 which is being recalled should return to place of purchase. 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 ”
Williamsburg Bridge, Brooklyn, NY, USA
June 13, 2020 12:40 PM
“Peaceful protest from Manhattan to Brooklyn ”
Symptoms: Diarrhea Vomiting
March 17, 2020 8:43 PM
“Interview - Maroy, Lyon France:
This is a first hand account of the coronavirus situation in Lyon France, including one member of their community that has been diagnosed, and another working in a nearby hospital.
I am 25 and I'm living in Lyon in the east France and it's like the third ... region which is the most touched by the virus. And right now I'm at home since Monday the government told us to stay at home, so I'm not touched by the virus, but I know some, an old person who are touched by the virus. And I have a friend who is working in the hospital in the care units and she explained to me what the media is hiding and what's the truth behind this virus.
What area does your friend work in the hospital? And what is she seeing?
She's living in the South of France, Toulouse and she's in the care units. So she's working closely with the people who are in the worst situation in the hospital. So she see's a lot of cases everyday and everyday she's told me that it's worse.
Some of the materials state that it's mostly older people that are impacted, is that what she's seeing?
So at first in the media, they say that only old people and fragile persons who have a disease are impacted. But now this is not the truth. Now,people who are 23 years old, 25, 30 are impacted.
Have you heard anything about testing? Is it hard to get testing or is it easy to get testing?
Yes. One week ago I was talking with my doctor and we were talking about the virus and he told me, you know, we are talking a lot with the other doctors and I can tell you right now that we don't have in France,no testing, no tests anymore. We don't know if a person has a flu, if it's simple flu or the coronavirus and when he told me that I was really anxious because even the doctors can't diagnose now if this only a flu or if it's worse.
At the hospital, where your friend works? Is there enough room for people or are they worried about how much space they have?
No, unfortunately not. Now they are transferring patients to another hospital to welcome the patients who are infected by the virus. And I also heard that in some hospitals they are taking the children's room. So the services reserved for children, they are transferred to the care unit because they do not have enough room for them. They don't have enough places now.
Is there anyone that you know of or any people that you are aware ofthat directly, or through friends or family that have been diagnosed with coronavirus?
Yes, the cousin of my husband has been diagnosed so she's at home. She can't be at the hospital because there are too many people and they said that if she don't have struggle to breathe, she needs to stay at home. The government said that you can call emergency, only if you're struggling to breathe, if you should just have fever. Or a cough if you cough you stay at home, but really if you can't breathe you can call the emergency.
So now that you've had experience in France with coronavirus, and hearing about your husband's cousin and your friend at the hospital, what's your feeling about coronavirus and how serious it is? Are you concerned now that you have had direct impact?
Yes. I'm really mad get the government because they they take that too easily. They didn't do the right things at the beginning. People need to understand that this is really, really serious. And I'm pretty anxious because now yesterday I was doing shopping, so just to buy food and the all people in the grocery was afraid was wearing masks and there was nothing, people were struggling to find some pasta or something like that. And I'm really mad because we can see that a lot and a lot of people are infected by the virus. My friend who is nurse, is really afraid, she's really anxious, she's really scared to have it. She's pregnant and she needs to work even if she's pregnant. And I'm really mad against the government for that. I'm sure that if it took the good decision at the right time, they would not have a lot of cases like right now.
Is there any message that you have for people listening based on what you've learnt so far?
Don't take that too lightly. This is really my word, don't take that too lightly. When I see that in UK, they say that they are counting on the auto immunity of people. I just don't understand. If I have a thing to say it, don't shake hands, don't hug someone, wash your hands carefully, and just take it this really, really seriously. Because this is not a simple flu. It's bigger than that. ”
Lupin Pharmaceuticals, Inc Metformin Hydrochloride Extended-release Tablets - recalled due to Detection of N-Nitrosodimethylamine (NDMA), USA
June 11, 2020 1:00 PM
“Company name: Lupin Pharmaceuticals, Inc
Brand name: Lupin
Product recalled: Metformin Hydrochloride Extended-release Tablets
Reason of the recall: Detection of N-Nitrosodimethylamine (NDMA)
FDA Recall date: June 11, 2020
Recall details: Lupin Pharmaceuticals Inc. is voluntarily recalling Met ... formin Hydrochloride Extended-Release Tablets USP (generic equivalent of Fortamet®), 500mg, lot G901203 to the consumer level. FDA analysis revealed that this lot exceeded the Acceptable Daily Intake Limit for the impurity N-Nitrosodimethylamine (NDMA). To date, Lupin Pharmaceuticals Inc. has not received any reports of adverse events related to 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 and found in water and foods, including meats, dairy products and vegetables. Metformin Hydrochloride Extended-Release Tablets USP, 500mg is a prescription oral medication indicated as an adjunct to diet and exercise to improve blood glucose control in adults with type 2 diabetes mellitus. It is packaged in a bottle containing 60 tablets with NDC 68180-336-07. The affected lot of Metformin Hydrochloride Extended-Release Tablets USP, 500mg is included in below table:
- Product Name: Metformin Hydrochloride Extended-Release Tablets USP, 500mg
- NDC: 68180-336-07
- Lot Number: G901203
- Expiration Date: 12/2020
The product can be identified by the NDC and the lot number available on the side of the bottle label. Metformin Hydrochloride Extended-Release Tablets USP, 500mg was distributed nationwide in the USA to wholesalers, distributors, and mail order pharmacies.
Lupin Pharmaceuticals Inc. is notifying its wholesalers, distributors, and mail order pharmacies by phone and through recall notification and is arranging for the return of all the recalled product lot. Patients taking Metformin Hydrochloride Extended-Release Tablets, USP 500 mg, 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.
Check the full recall details on fda.gov
Source: FDA ”
KFC, 35 Camberwell Church St, Camberwell, London SE5 8TR, United Kingdom, KFC, 35 Camberwell Church St, Camberwell, London SE5 8TR, United Kingdom
KFC, 35 Camberwell Church St, Camberwell, London SE5 8TR, United Kingdom
June 21, 2020 11:30 AM
“why am I being given raw chicken? ”
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.. ”
Braun Medical Inc Ceftazidime for Injection USP (2g) and Dextrose for Injection USP (50 ml) in Duplex® Container - recalled due to Out-of-Specification Results, B. Braun Medical Inc, 824 12th Avenue, Bethlehem, Pennsylvania 18018, USA
B. Braun Medical Inc, 824 12th Avenue, Bethlehem, Pennsylvania 18018, USA
April 20, 2020 6:00 PM
“Company name: Braun Medical Inc
Brand name: B. Braun
Product recalled: Ceftazidime for Injection USP (2g) and Dextrose for Injection USP (50 ml) in Duplex® Container
Reason of the recall: Out-of-Specification Results for High Molecular Weight Polymers
FDA Recall date: April 20, 2020
Recall de ... tails: Braun Medical Inc. (B. Braun) is voluntarily recalling one (1) lot of 2g Ceftazidime for Injection USP (2g) and Dextrose for Injection USP (50 ml) in Duplex® Container to the hospital/user level.. During stability testing of Batch H8J812, test results were found to exceed the specification limits for High Molecular Weight Polymers (HMWP) at the nineteen (19) month [82 week] stability interval. Elevated levels of High Molecular Weight Polymers have been shown to cause kidney damage and liver issues in animal studies. While the impact of HMWP in humans is unknown, B. Braun is initiating this voluntary recall out of an abundance of caution to prevent any risks of adverse reactions due to the elevated HMWP levels.
To date there have been no complaints or reports of adverse reactions associated with this product lot. Ceftazidime for Injection USP and Dextrose Injection USP is a cephalosporin antibacterial indicated in the treatment of the following infections caused by susceptible isolates of the designated microorganisms: Lower respiratory tract infections; skin and skin-structure infections; bacterial septicemia; bone and joint infections; gynecologic infections; intra-abdominal infections; and central nervous system infections.
Ceftazidime for Injection USP and Dextrose Injection USP in the DUPLEX® Container is a flexible dual chamber container containing approximately 50 mL of 5% Dextrose Injection in the diluent chamber and ceftazidime in the drug powder chamber. After reconstitution, the concentration is equivalent to 2 g ceftazidime. Ceftazidime for Injection USP and Dextrose Injection USP is packaged in 24 DUPLEX® Containers per case. The affected recalled product includes the following lot number and expiration date:
- NDC: 0264-3145-11. Ref: 3145-11. Dose/Volume: 2 g per 50 mL. Impacted batch: H8J812. Exp. Date: 31 Jul 2020.
Product was distributed Nationwide within the United States to domestic distributors. Pictures of the product and product labeling follow this press release.
B. Braun is notifying its distributors and customers by an official recall notice sent via certified registered mail and is arranging for return of all recalled products. Facilities and distributors that have product which is being recalled should discontinue use immediately and contact the B. Braun Medical Inc. Customer Support Department
Check the full recall details on fda.gov
Source: FDA ”
Chengdu Ai Qin Colored contact lenses - recalled due to being distributed without FDA clearance, USA
June 24, 2020 6:00 PM
“Company name: Chengdu Ai Qin E-commerce Co., Ltd
Brand name: TTDeye
Product recalled: Colored contact lenses
Reason of the recall: Distributed without FDA clearance may pose health risk
FDA Recall date: June 24, 2020
Recall details: On June 18, 2020, Chengdu Ai Qin E-commerce Co., Ltd initiate ... d a nationwide recall of 1362 pairs of colored contact lenses. The relevant series of contact lenses have been found to be distributed without FDA clearance and may pose a threat to health. The company has received no complaints to date.
These colored contact lenses were sold through the company website and shipped directly to the customer from 08/05/2019 - 10/11/2019. The recalled products were manufactured in August 2018 and may be identified by name of the product and the date of manufacture, “2018-08”, found on the package label. The following products are being recalled:
- TTDeye. Black Starshine. Lot code: B16112100
- TTDeye. Diamonds Starlight. Lot code: B16112203
- TTDeye. Flower. Lot code: Brown. Lot code: B16112210
- TTDeye. Flower Grey. Lot code: B16112231
- TTDeye. Radial. Lot code: Brown. Lot code: B16112109
- TTDeye. Radial Pink. Lot code: B16112110
- TTDeye. Devil Red. Lot code: B16112201
If you have received this product, immediately cease use and contact the company via online chat at www.ttdeye.com between 9AM and 6PM (GMT+8) or contact the company via email at firstname.lastname@example.org (24 hours) for further information.
Chengdu Ai Qin E-commerce Co., Ltd is notifying its customers by email and is arranging for return/replacement of all recalled colored contact lenses.
Chengdu Ai Qin E-commerce Co., Ltd is voluntarily recalling these contact lenses after becoming aware of the problem. Chengdu Ai Qin E-commerce Co., Ltd has notified the FDA of this action.
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 ”