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
Total all time reports:
1
Latest report: July 16, 2020 12:00 PM
ZL
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
814
Related Reports
33 employees tested positive for Covid-19, Oregon State Penitentiary,2605 State St, Salem, OR 97310
1 week ago
33 employees tested positive for Covid-19 at Oregon State Penitentiary in Marion County. Investigation Start Date: 7/7/2021, with the most recent onset of: 9/29/2021 New Cases of: 33
Source: www.oregon.gov See Less
988
161 employees tested positive for Covid-19 at Sheridan Federal Correctional Institution in Yamhill County. Investigation Start Date: 7/29/2021, with the most recent onset of: 9/25/2021 New Cases of: 161
Source: www.oregon.gov See Less
988
23 employees tested positive for Covid-19 at Shutter Creek Correctional Institution in Coos County. Investigation Start Date: 8/11/2021, with the most recent onset of: 9/25/2021 New Cases of: 23
Source: www.oregon.gov See Less
21
14 employees tested positive for Covid-19 at Siskiyou Community Health Center in Josephine County. Investigation Start Date: 7/26/2021, with the most recent onset of: 9/21/2021 New Cases of: 14
Source: www.oregon.gov See Less
129
39 employees tested positive for Covid-19 at Snake River Correctional Institution in Malheur County. Investigation Start Date: 7/19/2021, with the most recent onset of: 10/2/2021 New Cases of: 39
Source: www.oregon.gov See Less
94
36 employees tested positive for Covid-19 at Sysco Portland in Clackamas County. Investigation Start Date: 8/2/2021, with the most recent onset of: 10/3/2021 New Cases of: 36
Source: www.oregon.gov See Less
988
7 employees tested positive for Covid-19, The Home Depot,4999 Depot Ct SE, Salem, OR 97302
1 week ago
7 employees tested positive for Covid-19 at The Home Depot in Marion County. Investigation Start Date: 10/7/2021, with the most recent onset of: 10/3/2021 New Cases of: 7
Source: www.oregon.gov See Less
988
23 employees tested positive for Covid-19 at Two Rivers Correctional Institute in Umatilla County. Investigation Start Date: 7/15/2021, with the most recent onset of: 9/20/2021 New Cases of: 23
Source: www.oregon.gov See Less
100
5 employees tested positive for Covid-19 at Walmart in Marion County. Investigation Start Date: 10/6/2021, with the most recent onset of: 10/3/2021 New Cases of: 5
Source: www.oregon.gov See Less
988
LA Fitness, Lawrence, NY, USA
1 week ago
I recently returned to this gym for the first time since it was locked down in March 2020. I’ve been going for 3 days a week for two weeks straight and not once was I asked for proof of my vaccination status. There seem to be no... See More enforcement of COVID protocols including requiring proof of vaccination, distancing, or consistent cleaning. See Less
5.1K
Recent Interesting Reports
Emergen-C Energy Release & Immunity Support - recalled due to unauthorized pesticide, Ireland
1 week ago
The FSAI announced the recall of certain batches of Emergen-C Energy Release and Immunity Support Food Supplement due to the presence of the unauthorized pesticide ethylene oxide. Ethylene oxide is a pesticide that is not permitted for use in foods sold in the EU but is approved... See More for use by other countries outside the EU.
The recalled products are:
- Emergen-C Energy Release & Immunity Support Super Orange, Mega Pack 24 sachets, Lot # FUB03, Best before 01/24.
- Emergen-C Energy Release & Immunity Support Super Orange, Mega Pack 24 sachets, Lot # NT489, Best before 10/23.
- Emergen-C Energy Release & Immunity Support Super Orange, 8 sachets, Lot # GU393, Best before 10/23.
Although the consumption of the contaminated product does not pose an acute risk to health, there is an increased risk if there is continued consumption of contaminated food over a long period of time. Therefore, exposure to this substance needs to be minimised.
For more recall details check on FSAI website: fsai.ie
Source: FSAI See Less
5
It’s been over 20 days for next-state packages and still have not arrived. See Less
5.1K
Company name: Cook Medical
Brand name: Cook Medical
Product recalled: Transseptal Needle and Transseptal Needle Catheter
Reason of the recall: Complaints of rust on the products
FDA Recall date: October 19, 2021
Recall details: Bloomington, Ind. — On October 8, 2021, Cook Medical issued a global, voluntary... See More recall of the Transseptal Needle and the Transseptal Needle with Catheter. This recall includes all unexpired lots for both of these products. The needles were recalled due to complaints of rust on the products. Use of affected products could result in increased procedural time and inflammatory reactions, including systemic reactions which may lead to permanent impairment or death.
The U.S. Food and Drug Administration (FDA) has not yet classified the recall. Products affected by this recall are:
- Transseptal Needle, INTENDED USE: Intended for transseptal left heart access in both diagnostic and interventional procedures, RPN: TSNC-18-71.0 GPN: G02364 and RPN: TSNC-19-56.0 GPN: G02365, all lot numbers, RANGE OF MANUFACTURE DATES FOR AFFECTED PRODUCTS: October 02, 2016 through July 22, 2021
- Transseptal Needle with Catheter, INTENDED USE: Intended to facilitate transseptal entry into the left atrium, RPN: TSN-17-75.0-ENDRYS, GPN: G19261, all lot numbers, RANGE OF MANUFACTURE DATES FOR AFFECTED PRODUCTS: October 02, 2016 through July 22, 2021
Transseptal Needles, including Transseptal Needles with Catheters, were found to have rust internally, externally, or both. To date, Cook Medical has received no reports of injury or illness related to this recall. Cook has received four complaints where the presence of rust was identified prior to patient contact. However, please be advised that the presence of rust may go undetected by the user. The FDA and other regulatory agencies around the world have been notified of this action.
Potential adverse events: If an affected product is used, potential negative outcomes include increased procedural time (to obtain a replacement device) and inflammatory reactions ranging from local or self-limited reactions to systemic reactions requiring medical intervention. Systemic reactions could potentially lead to permanent impairment or death.
Check the full recall details on fda.gov
Source: FDA See Less
97
I ordered a hand held battery powered mini chainsaw in March this year but haven’t received it as yet but I got a wire cutting which is useless and I want my money returned as I think I have been very patient but nearly 6 months is... See More plenty of time to honor.
I have a copy of my receipt and confirmation and I also am sorry that this has been happening to other people | Symptoms: Other See Less
A few weeks ago. My cat got sick from food delivered by chewy. It sat on the porch in the sun. It is wet food. We noticed the color was off but didn’t think it could make him so sick. I had to take him to the... See More vet twice for vomiting and not eating after 1 can. I emailed chewy and sent pictures. They refunded my money and I will only go to the pet store for food for now on. | Symptoms: Nausea, Vomiting See Less
3.7K
Company name: Eli Lilly and Company
Brand name: Lilly
Product recalled: Glucagon Emergency Kit
Reason of the recall: Loss of potency
FDA Recall date: September 26, 2021
Recall details: Eli Lilly and Company (NYSE: LLY) is voluntarily recalling lot D239382D, Expiration April 2022, of Glucagon Emergency Kit... See More for Low Blood Sugar (Glucagon for Injection, 1 mg per vial; Diluent for Glucagon, 1 mL syringe), to the consumer/user level. Lilly is recalling lot D239382D to the patient level because of a product complaint reporting that the vial of Glucagon was in liquid form instead of the powder form.
The firm’s investigation indicates that the liquid in this Glucagon vial could be related to the manufacturing process. The use of the liquid form of this product may fail to treat severe low blood sugar due to loss of potency.
Risk Statement: Severe hypoglycemia in patients with diabetes, if not reversed, can potentially cause adverse health consequences ranging from transient, minor complaints to neurological damage, seizures, and even death if not promptly treated. Associated with the one product complaint, it was reported to Lilly that the involved patient experienced lack of drug effect and also reported subsequent seizures.
Glucagon Emergency Kit is used as an anti-hypoglycemic agent and a gastrointestinal motility inhibitor indicated for the treatment of severe hypoglycemia in pediatric and adult patients with diabetes mellitus. The product is packaged in a kit containing 1mg of freeze-dried (lyophilized) product in a 3 mL vial and a pre-filled diluent syringe. The affected Glucagon Emergency Kit lot is D239382D and the expiration date is April 2022 (label expiry date: 04 2022). The lot number can be found on the label of the kit as well as the vial (refer to the photos provided below – Appendix A). The lot was distributed nationwide to wholesalers and retailers.
Wholesalers and Distributors with an existing inventory of Glucagon Emergency Kit lot D239382D should cease distribution and quarantine the product immediately.
Instructions for Wholesalers and Pharmacists: If you have distributed the recalled product, please notify any accounts or additional locations which may have received product from the recalled lot from you. Please conduct a sub-recall to those accounts and communicate this recall information immediately.
Instructions for Consumers: Consumers in possession of Glucagon Emergency Kit lot D239382D should contact The Lilly Answers Center at 1-800-545-5979 for return and replacement instructions for the product (hours of operation are Monday- Friday, 9AM – 7PM EST) and should contact their health care provider for guidance. 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. APPENDIX A The Lot Number is found on the kit and vial labels as can be seen in the example label below.
Check the full recall details on fda.gov
Source: FDA See Less
97
Waiting on a package , USPS Teterboro Distribution Center, Industrial Avenue, Teterboro, NJ, USA
3 weeks ago
Bronx. Wagon a package saying in transit since Saturday from teterboro See Less
5.1K
Fromm Four-Star Nutritionals Shredded Entrée dog food - recalled due to high Vitamin D, USA
3 weeks ago
FROMM FAMILY FOODS is issuing a voluntary recall of approximately 5,500 cases of Fromm Shredded can Entrée dog food due to potentially elevated levels of Vitamin D.
Consumers should stop feeding the products listed below to their dogs. Potential adverse reactions could occur in all size dogs. ... See More No reports of illness or injury have been reported from consumers to date, however Fromm management has determined it is prudent to pull these four lots out of distribution.
Affected recalled products were distributed at neighborhood pet stores nationwide.
Products are packaged in 12 oz. cans with Best By Date 08/2024. A full list of affected products is:
- Four-Star SHREDDED BEEF IN GRAVY ENTRÉE food for dogs, 12 cans per case, 11877, 12 oz. per can, UPC: 7270511876, Best By Date 082024
- Four-Star SHREDDED CHICKEN IN GRAVY ENTRÉE food for dogs, 12 cans per case, 11881, 12 oz. per can, UPC: 7270511880, Best By Date 082024
- Four-Star SHREDDED CHICKEN IN GRAVY ENTRÉE food for dogs, 12 cans per case, 11879, 12 oz. per can, UPC: 7270511878, Best By Date 082024
-Four-Star SHREDDED TURKEY IN GRAVY ENTRÉE food for dogs, 12 cans per case, 11883, 12 oz. per can, UPC: 7270511882, Best By Date 082024
Dogs ingesting elevated levels of Vitamin D may exhibit symptoms such as vomiting, loss of appetite, increased thirst, increased urination, excessive drooling, and weight loss. Vitamin D when consumed at very high levels can lead to serious health issues in dogs including renal dysfunction. Consumers who have dogs that have consumed any of the affected products and are exhibiting these symptoms should contact their veterinarian.
Check the full recall details on fda.gov
Company name: Fromm Family Foods
Brand name: Fromm Four-Star Nutritionals
Product recalled: Shredded Entrée canned dog food
Reason of the recall: Elevated levels of Vitamin D
FDA Recall date: October 01, 2021
Source: FDA See Less
97
Shipment was supposed to arrive Friday. Now I received the following message : Your shipment has potentially been delayed due to emergency or other conditions at 6:46 pm on October 17, 2021. | Symptoms: Other See Less
5.1K
GR
Grinsler
Same here. Mine arrived at Teterboro 10/14 @ 3:35 pm. 10/17 update says "Processing Exception, Other Delay Your shipment has potentially been delayed due to emergency or other conditions at 6:50 pm on October 17, 2021."
MI
This is the 2nd package that just arrives at teterboro and just stops moving what’s the point of charging for next day air if you can’t get it done .. worse thing about this is that’s it’s anxiety medication i desperately need See Less
5.1K
HA
Hate USPS
I wonder if we could all group together and file a class action lawsuit. I saw another post here with two tracking #s stuck from October 1st and Sept 28th that haven’t moved yet.