Report by
Thank you for your report!
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)
If your report is poison related call
1-800-222-1222
for a free consultation with a live medical poisoning expert
Visit our learn pages for more helpful information or, email us:
support@safelyhq.com
Goodbye! and best wishes in your recovery
Melt Bar and Grilled, 3921 Medina Rd, Akron, OH 44333, USA
Latest report: July 16, 2020 12:00 PM
SN
Employee test positive for Covid-19
1 year ago
An employee at the Melt Bar and Grilled in Akron tested positive for COVID-19.
Source: fox8.com See Less
1.0K
Related Reports
Multiple employees(3) at VCA VETERINARY CARE ANIMAL HSP in ALBUQUERQUE, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 06/28/2022,
Source: env.nm.gov See Less
451
Multiple employees(2) at VCA WEST MESA ANIMAL HOSPITAL in ALBUQUERQUE, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 06/28/2022,
Source: env.nm.gov See Less
451
Multiple employees(2) at WALGREENS in ROSWELL, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 06/28/2022,
Source: env.nm.gov See Less
17
2 employees tested positive for Covid-19, WALMART PHARMACY, 3500 COORS BLVD SW, ALBUQUERQUE, NM
2 days ago
Multiple employees(2) at WALMART PHARMACY in ALBUQUERQUE, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 06/28/2022,
Source: env.nm.gov See Less
451
1 employee tested positive for Covid-19, WALMART SUPERCENTER, 1650 W MALONEY AVE, GALLUP, NM
2 days ago
An employee(1) at WALMART SUPERCENTER in GALLUP, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 06/28/2022,
Source: env.nm.gov See Less
8
3 employees tested positive for Covid-19, WALMART SUPERCENTER, 2250 MAIN ST NW, LOS LUNAS, NM
2 days ago
Multiple employees(3) at WALMART SUPERCENTER in LOS LUNAS, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 06/28/2022,
Source: env.nm.gov See Less
451
2 employees tested positive for Covid-19, WALMART SUPERCENTER, 2550 COORS BLVD NW, ALBUQUERQUE, NM
2 days ago
Multiple employees(2) at WALMART SUPERCENTER in ALBUQUERQUE, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 06/28/2022,
Source: env.nm.gov See Less
451
2 employees tested positive for Covid-19, WALMART SUPERCENTER, 2609 7TH ST, LAS VEGAS, NM
2 days ago
Multiple employees(2) at WALMART SUPERCENTER in LAS VEGAS, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 06/28/2022,
Source: env.nm.gov See Less
15
2 employees tested positive for Covid-19, WALMART SUPERCENTER, 400 EUBANK BLVD NE, ALBUQUERQUE, NM
2 days ago
Multiple employees(2) at WALMART SUPERCENTER in ALBUQUERQUE, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 06/28/2022,
Source: env.nm.gov See Less
451
2 employees tested positive for Covid-19, WHOLE FOODS MARKET, 753 CERRILLOS RD, SANTA FE, NM
2 days ago
Multiple employees(2) at WHOLE FOODS MARKET in SANTA FE, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 06/28/2022,
Source: env.nm.gov See Less
124
Recent Interesting Reports
I just opened my bag of dream ones and there is black mold on the bones, Glendale, AZ, USA
1 week ago
as I stated before, I just opened a brand new bag of Dreambones and saw that there is black mold on the bones See Less
1.0K
Nottingham, NH, Buzzagogo Inc. is voluntarily recalling one lot of Allergy Bee Gone for Kids Nasal Swab Remedy to the consumer level due to potential microbial contamination. FDA testing found some product to contain elevated levels of yeast & mold and may contain the bacteria Bacillus cereus.... See More Allergy Bee Gone for Kids Nasal Swab Remedy, lot # 2006491, was distributed Nationwide to wholesale distributors, retail stores and online on Amazon.com and the company web site. Buzzagogo, Inc. places the utmost emphasis on patient safety and product quality at every step in the manufacturing and supply chain process.
Risk Statement: In immunocompromised patients, the use of the affected product could potentially result in severe or life-threatening adverse events such as bacteremia/sepsis, pneumonia, invasive fungal rhinosinusitis, or disseminated fungal infection. In non-immunocompromised patients, the population most likely to use the product, the use of the defective product may result in infectious complications, for instance bacteremia or noninvasive fungal rhinosinusitis, but in this population the infections are expected to be less severe and more readily responsive to treatment. To date, Buzzagogo, Inc. has not received any complaints related to microbial concerns or reports of adverse events related to this recalled lot.
The product is used to lessen seasonal allergy symptoms and is packaged in individual tubes for topical nasal application. The affected Allergy Bee Gone for Kids Nasal Swab Remedy lot is 2006491 with expiration date 8/2024 and UPC code 860002022116. The product can be identified by locating the lot number and expiration date on the bottom of the product carton.
Buzzagogo, Inc. is notifying its distributors and customers by email and is arranging for return or replacement of all recalled products. Consumers, distributors or retailers that have Allergy Bee Gone for Kids Nasal Swab Remedy, lot # 2006491, should stop using the product, and discard any remaining product.
Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to using this drug product.
Company name: Buzzagogo Inc.
Brand name: Allergy Bee Gone for Kids
Product recalled: Nasal Swab Remedy
Reason of the recall: Product contains elevated levels of Bacillus cereus
FDA Recall date: June 07, 2022
Source: fda.gov See Less
440
Power outage, 9508 U.S. 24, Fort Wayne, IN, USA
2 weeks ago
We have been without power since Monday night, this is so uncomfortable having no power along with this high heat and humidity. Even had to throw out the food in the refrigerator. We don’t even have water because of a pump that takes electricity. Thank you See Less
271
1.5 years no tenant. Overgrown lawn, door falling off hinges. Lowering property values and turning area into ghetto See Less
404
Bryant Ranch Prepack Inc. is voluntarily recalling one lot of Morphine Sulfate 30 mg Extended-Release tablets (Comprised of 10 bottles), and one lot of Morphine Sulfate 60 mg Extended-Release tablets (Comprised of 10 bottles) to the consumer level listed below. The products have been found to have... See More incorrect labeling where bottles labeled as Morphine Sulfate 60 mg Extended-Release tablets contain Morphine Sulfate 30 mg Extended-Release tablets and bottles labeled as Morphine Sulfate 30 mg Extended-Release tablets may contain Morphine Sulfate 60 mg Extended-Release tablets.
Risk Statement: Patients prescribed the 30 mg dose who receive the 60 mg dose could be at risk for overdose and death. Patients prescribed the 60 mg dose who receive the 30 mg dose may experience withdrawal and untreated pain if the dose given is too low. To date, Bryant Ranch Prepack Inc. has not received any reports of adverse events related to this recall.
-Affected products:
Product: Morphine Sulfate Extended-Release Tablets
Strength: 30 mg
Quantity per bottle: 100
NDC: 63629-1088-01
Lot: 179642
Expiration: 11/30/2023
Product: Morphine Sulfate Extended-Release Tablets
Strength: 60 mg
Quantity per bottle: 100
NDC: 63629-1089-01
Lot: 179643
Expiration: 08/31/2023
Morphine Sulfate Extended-Release tablets are used to manage severe pain. The 30 mg tablets are round, purple-colored, film-coated tablets debossed with "RD" and "71" on one side and plain on the other side. The 60 mg tablets are round, light orange-colored, film-coated tablets debossed with "RD" and "72" on one side and plain on the other side.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
In case you experienced harm from this product, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance.
Company name: Bryant Ranch Prepack Inc.
Brand name: Bryant Ranch Prepack Inc.
Product recalled: Morphine Sulfate 30 mg Extended-Release tablets
Reason of the recall: Incorrect labeling
FDA Recall date: June 29, 2022
Source: fda.gov See Less
440
Power outage at the Baymont hotel in Baxter, MN See Less
104
Dreambone, Fredericktown, MO, USA
1 week ago
My baby princess is five years old. I used to get her good n fun kabobs and about a six months ago she tried the dreambone wrapped in chicken and she liked them alot and I have been buying them at 18 dollars a bag to make... See More my baby very sick in so many ways she has choking problems she has been having blood in her poop and is deathly sick now. Remind you at the end of the day I don't have anyone else she is it. I hold on to her and she's very spoiled and is why I wake up and work and she's my world. I had her mom 10 years and I didn't know that it was the treats. I let her eat as much of them as 30 in day and I feel aweful and this company is wrong and I am not going to stop until something is done about it I just really am in shock. My mom called 911 even one day she was choking. I could not imagine the thought of losing her. I've had her serviced and I've lost twins and she is a child and every single pet parents in the world is about to get the truth of this place because it's terrible and dreambone shouldn't be doing this. At almost $20 a bag at that. This place needs to be stopped and not all people can always afford the vet and struggle everyday and lives are hard enough without the worry and deaths of our pets.i can't even believe people are doing this seriously. | Symptoms: Bloody Stool See Less
87
Green Pharmaceuticals Inc is voluntarily recalling lot 2373/21222 of SnoreStop NasoSpray, packaged in 0.3 FL OZ (9ml) bottles to the consumer level. FDA testing found product to contain microbial contamination identified as Providencia rettgeri. To date, Green Pharmaceuticals Inc has not received any reports of adverse events... See More related to this recalled lot.
This microorganism is rarely associated with human illness; however, in immunocompromised patients, the use of the recalled product could potentially result in severe or life-threatening adverse events such as bacteremia/sepsis, pneumonia, invasive fungal rhinosinusitis, or disseminated fungal infection. In non-immunocompromised patients, the use of the recalled product may result in infectious complications that are expected to be less severe and more readily responsive to treatment.
The product is used as a nasal spray to temporarily help stop or reduce symptoms of non-apneic snoring and is packaged in one single unit plastic bottle with a nasal pump as a delivery system. The affected SnoreStop NasoSpray lot includes the following: 2372/21222 (2373 is printed on a sticker placed on the bottom of the bottle and 21222 is on a sticker placed on the outer packaging).
The product can be identified by a clear transparent plastic box with the name SnoreStop NasoSpray. The product was distributed nationwide in health food stores and online. Green Pharmaceuticals Inc is notifying its retailers and customers by email and is arranging for return and replacement of all recalled products. Consumers and retailers that have product which is being recalled should stop using and return to place of purchase.
Consumers with questions regarding this recall can contact Green Pharmaceuticals Inc by phone at 805-388- 0600, Monday through Friday, 8 AM to 5 PM Pacific Standard 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.
Company name: Green Pharmaceuticals Inc
Brand name: SnoreStop
Product recalled: Nasal spray
Reason of the recall: Due to microbial contamination identified as Providencia rettgeri.
FDA Recall date: June 09, 2022
Source: fda.gov See Less
440
Power outage Holloway Street and Hardy Street no street lights no traffic lights See Less
1.2K
Last 30 days