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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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H-E-B, San Antonio, TX 78257, United States

Total all time reports:  3
Latest report: July 2, 2020 12:00 PM
Employee has tested positive for Covid-19, H-E-B, San Antonio, TX 78257, United States

Employee has tested positive for Covid-19

July 2, 2020 12:00 PM

“The employee who tested positive for COVID-19 was last working in the store on 24165 I-10 West, Suite 300 on Friday, June 19. If you visited the supermarket recently, please report it and any other location that you visited.

Source: mysananto ... See Morenio.com See Less
Reported By SafelyHQ.com User

Employee test positive for Covid-19

June 28, 2020 12:00 PM

“An H-E-B employee at the 24165 I-H 10 West location tested positive for COVID-19 and last worked on Monday, June 15.

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

Employee test positive for COVID-19

June 17, 2020 12:00 PM

“An employee at the Leon Springs H‑E‑B on I-H 10 West tested positive for COVID-19 on June 8. If you visited the supermarket location during that time, please report it and any other location that you visited.

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

Related Reports

July 10, 2020 4:21 PM

“The company has had a worker test positive for covid-19 after being around other workers and letting the worker return back without retesting! The company won’t send any other workers to get tested because they don’t wanna pay or lose money, risking everyones health! The company is sorry and selfles ... See Mores! See Less
Reported By SafelyHQ.com User

July 9, 2020 12:10 PM

“I work at old navy and I have to tell security everyday to put on their mask. They never wear their mask like ever. I do believe they lied about having the right filtration system just so they can open See Less
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July 9, 2020 12:00 PM

“A Minco School district employee at the Summer Pride program has tested positive for COVID-19 and anyone who attended between June 22-25 should monitor for symptoms and report it.

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

Employee test positive for Covid-19, Hartsfield-Jackson Atlanta International Airport (ATL), North Terminal Parkway, Atlanta, GA, USA

Hartsfield-Jackson Atlanta International Airport (ATL), North Terminal Parkway, Atlanta, GA, USA

July 9, 2020 12:00 PM

“A TSA employee at the main security checkpoint at Hartsfield-Jackson Atlanta airport tested positive for COVID-19.



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

Employee test positive for Covid-19, Strip District Meats, Inc., 2123 Penn Ave, Pittsburgh, PA 15222, USA

Strip District Meats, Inc., 2123 Penn Ave, Pittsburgh, PA 15222, USA

July 9, 2020 12:00 PM

“An employee at Strip District Meats along Penn Avenue in Pittsburg tested positive for COVID-19

Source: pittsburgh.cbslocal.com See Less
Reported By SafelyHQ.com User

July 9, 2020 12:00 PM

“A small amount of employees at Berkeley Bowl West at 920 Heinz Ave. in Berkeley tested positive for Covid-19 on July 1. Both Berkeley ... See Morele="Product: Bowl">Bowl locations have had employees test positive for the coronavirus.

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

Employee test positive for Covid-19, Mj's Raw Bar and Grille, 216 Middle St, New Bern, NC 28560, United States

Mj's Raw Bar and Grille, 216 Middle St, New Bern, NC 28560, United States

July 9, 2020 12:00 PM

“An employee at MJ’s Raw Bar and Grille in downtown New Bern has tested positive for COVID-19.

Source: wcti12.com See Less
Reported By SafelyHQ.com User

Employee test positive for Covid-19, Shoshone-Bannock Casino Hotel, Ross Fork Rd, Pocatello, ID 83202, USA

Shoshone-Bannock Casino Hotel, Ross Fork Rd, Pocatello, ID 83202, USA

July 9, 2020 12:00 PM

“A Shoshone-Bannock Casino Hotel employee has tested positive for COVID-19.

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

July 9, 2020 12:00 PM

“A staff members at The Henry in Coronado tested positive for COVID-19. The last time the employee worked onsite was Tuesday, June 30th


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

July 9, 2020 12:00 PM

“One employee at Egg and U in Parker has tested positive for COVID-19 on July 6 after being sent home with symptoms.

Source: centennialcitizen.net ... See More See Less
Reported By SafelyHQ.com User

Recent Interesting Reports

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 ... See Moredetails: 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
- CMExpress

*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
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Reported By SafelyHQ.com User

June 18, 2020 11:00 PM

“Company name: GSK Consumer Healthcare
Brand name: Robitussin
Product recalled: Cough and cold products
Reason of the recall: Incorrect dosing cups
FDA Recall date: June 18, 2020
Recall details: GSK Consumer Healthcare is voluntarily recalling to the retail level two lots (listed below) of Ch ... See Moreildren's Robitussin® Honey Cough and Chest Congestion DM and one lot of Children's Dimetapp® Cold and Cough, due to the inclusion of incorrect dosing cups. During the review of the packaging documents for these products, GSK discovered that the dosing cups for the Children's Robitussin® Honey product are missing the 5 mL and 10 mL graduations, while the dosing cups for the Children's Dimetapp® product are missing the 10 mL graduation. The dosing cups packaged with both products only have the 20 mL graduation.

There is a potential risk of accidental overdose if caregivers dispensing the syrup do not notice the discrepancies between the graduations printed on the dosing cups and the indicated amounts to be administered (as directed in the instructions for use). Children's Robitussin Honey Cough & Chest Congestion DM contains 10 mg dextromethorphan HBr USP and guaifenesin USP 100 mg per 10 mL, and is labeled for children 4 and older, as well as adults. Children's Dimetapp Cold & Cough contains 2 mg brompheniramine maleate USP, 10 mg dextromethorphan HBr USP, and 5 mg phenylephrine HCl USP per 10 mL, and is labeled for children 6 and older, as well as adults.

Symptoms of overdose of either product may include any of the following: impaired coordination; brain stimulation causing increase in energy, elevation in blood pressure, heart rate, and respiration; a lack of energy and enthusiasm; severe dizziness or drowsiness; slow heart rate; fainting; psychotic behaviour; restlessness; seizure; decreased respiration; nausea; vomiting; constipation; diarrhea; abdominal pain; visual and hearing hallucinations; urinary retention.

As of the date of the recall announcement, GSK Consumer Healthcare has not received any adverse events related to these products or consumer complaints regarding the incorrect dosing cups supplied with the product. The recall is limited to the three lots listed below:

Children's Robitussin® Honey Cough and Chest Congestion DM (4oz)
NDC 0031-8760-12
Lots: 02177 (Exp. Jan. 2022) / 02178 (Exp. Jan. 2022)

Children's Dimetapp® Cold and Cough (8oz)
NDC 0031-2234-19
Lot: CL8292 (Exp. Sep. 2021)

These lots were distributed nationwide between February 5, 2020 and June 3, 2020 within the United States. GSK Consumer Healthcare has notified wholesalers, distributors and retailers to arrange for return of any recalled product. Wholesalers, distributors and retailers with an existing inventory of the lots being recalled should stop distribution and quarantine these lots immediately.

Wholesalers, distributors and retailers that have further distributed the recalled product should notify any accounts or additional locations which may have received the recalled product from them. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using 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.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration. In December 2018, GlaxoSmithKline plc reached an agreement with Pfizer, Inc. to combine their consumer health businesses into a new Joint Venture. August 01, 2019 was the first day of the new GSK Consumer Healthcare Joint Venture. Thus, when identifying impacted product, please be aware the Pfizer company name will still be present on the label.

Check the full recall details on fda.gov

Source: FDA
See Less
Reported By SafelyHQ.com User

July 6, 2020 11:33 AM

“not a good look... I was served pretty much raw chicken 🤢🤮 See Less
Reported By SafelyHQ.com User

June 22, 2020 5:43 PM

“just came to a 24 hour location and then quarter pounder is cold and raw help!!! should I be worried about food poisoning ???! This is disgusting See Less
Reported By SafelyHQ.com User

May 27, 2020 9:34 AM

“No chips with my meal and pink chicken Face with symbols over mouth Absolutely grim man See Less
Reported By SafelyHQ.com User

May 20, 2020 11:00 PM

“Company name: Kent Nutrition Group
Brand name: Kent
Product recalled: Home Fresh Starter AMP Crumble
Reason of the recall: Elevated Salt Levels
FDA Recall date: May 20, 2020
Recall details: Company Announcement Kent Nutrition Group (KNG) of Muscatine, Iowa is voluntarily recalling 27- 25 lb.bag ... See Mores of Home Fresh Starter AMP Crumble from a single batch due to elevated salt levels, which can present illness or death to poultry. Kent Nutrition Group has ceased distribution of this lot as FDA and the company continue their investigation. Potential health risks of elevated salt levels include decreased growth rate, increased thirst, weakness, difficulty walking, difficulty breathing and death. To date, KNG has received three complaints concerning this product, which included illnesses and deaths in broilers age 12-20 weeks. This lot was manufactured at the KNG Columbus, NE plant and includes product distributed to select DO IT® Best Hardware Stores in Oregon, Washington, California, Montana and Idaho. Product subject to the recall can be identified by product code 3487 and is identified by the lot code 1020031 stamped onto the white strip sewn used to seal the package. The company is working closely with the Food and Drug Administration (FDA) to further investigate this issue and ensure the recalled products are removed from store shelves and are no longer distributed. Customers who want Information on what to do with the product and or for more information can call Kent Nutrition Group Customer Service at 1-866-647-1212 Monday through Friday from 8 AM to 5 PM Central Time. Customers who have purchased Home Fresh Starter AMP Crumbles lot #1020031 are urged to dispose of or return it to the place of purchase for a full refund.
Check the full recall details on fda.gov
Source: FDA
See Less
Reported By SafelyHQ.com User

March 25, 2020 12:41 PM

“The company’s Soho location closed earlier this week. The employee who tested positive for COVID-19 was last in the Soho store on Tuesday, March 17, according to a company spokesperson. It’s still up-in-the-air when the Soho Trader Joe’s will reopen, but standard protocol is to close at least three ... See Moredays for cleaning.

“Out of an abundance of caution, we have temporarily closed the store for thorough cleaning and sanitization. As soon as the store has been fully cleaned and restocked, we plan to reopen,” Trader Joe’s said in an announcement on their website.
Source: ny.eater.com
See Less
Reported By SafelyHQ.com User

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 ... See Morefelyhq.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 See Less
Reported By SafelyHQ.com User

Bike Protest, Williamsburg Bridge, Brooklyn, NY, USA

Williamsburg Bridge, Brooklyn, NY, USA

June 13, 2020 12:40 PM

“Peaceful protest from Manhattan to Brooklyn See Less
Reported By SafelyHQ.com User

June 17, 2020 12:36 PM

“Organic Banana, had real strings (thread) inside See Less
Reported By SafelyHQ.com User