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Little Caesars Pizza, Cleveland Ave, Columbus, OH, USA
Employees not wearing gloves or mask
1 year ago
The pizza When i got my pizza at drive threw noone had gloves or a mask on the girl at the window keep rubbing her nose i seen a guy making pizxa sneeze while making pizza i should have known better when i ask why noone had... glove or mask i was told when the pizza go in the oven the oven kills all germs i was told by cashier i got sick and my wife also
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... enforcement of COVID protocols including requiring proof of vaccination, distancing, or consistent cleaning.
Eastern Bartholomew Water Company has issued a boil water advisory for some of its customers due to water main maintenance.
The affected area include County Road 500E at State Road 46 to County Road 300S and 600E, along with County Road 200S to Burnsville.
Source... publication date: 2021 09 16
Due to maintenance on a water line in the Hamour Heights Subdivision, customers from County Road 600E at State Road 46 to County Road 300S at 600 East will be under a water boil advisory until Thursday at 4 p.m
Source publication date: 2021 09... 14
1 month ago
Multiple employees(2) at COLUMBUS ELEMENTARY in DEMING, NM tested positive for Covid-19 and the company is on the Rapid Response COVID-19 Watchlist Event Date: 09/15/2021,
1 month ago
Employees must drive company trucks and trucks are not always assigned to the same person. No procedures in place to ensure trucks are sanitized before each use, Covid-19 concerns.
Source: Osha.gov | Receipt Date: 2020-11-20
Employees are exposed to health hazards associated with the SARS-CoV-2 virus, in that the employer is not implementing Centers for Disease Control and Prevention (CDC) guidelines including quarantining employees with symptoms or positive for COVID-19 and advising co-workers when they may have been exposed to a contagious... individual. Location: The whole facility.
Alleged Hazards: 1, Employees Exposed: 10
Source: Osha.gov | Receipt Date: 2021-08-16
Multiple employeess in the store have tested positive with Covid, not contact tracing. All of management do not wear masks. An employee is currently working that is visibly sick. No precautions are being taken to stop the spread of COVID for employees.
Source: Osha.gov | Receipt Date: 2020-11-12
Covid-19 OSHA Complaint, Appian Manufacturing Corporation, 2025 Camero Avenue, COLUMBUS, OH, 43207, USA
1 month ago
Complaint: Employees are working with hazardous chemicals without the appropriate PPE Findings: The employer had conducted a hazard assessment and determined what PPE was required for each task. Employees interviewed stated that they had all the PPE they needed for working with chemicals. No citation issued. Complaint:... The employer has not taken the appropriate steps to protect employees from SARS-CoV-2, the virus that causes COVID-19 including but not limited to having employees wear masks and taking temperatures. Findings: The employer required masks for employees when 6 feet of distance could not be maintained. The employer had a thermometer available for use on site if needed, but employees were expected to monitor symptoms and not report to work if ill. Employees who tested positive for COVID-19 were also offered PTO. No citation issued.
Source: Osha.gov | Receipt Date: 2021-05-12
Covid-19 OSHA Complaint, Columbus Marble Works, Inc, 2415 Highway 45 North, COLUMBUS, MS, 39705, USA
1 month ago
1. Employees are not notified when an employee test positive for COVID-19. 2. Hand sanitizer is not available in work areas. 3. The work area is not sanitized for COVID-19.
Alleged Hazards: 3, Employees Exposed: 53
Source: Osha.gov | Receipt Date: 2021-08-02
Columbus City Utilities has issued a precautionary boil water advisory for customers in an area off of Marr Road near Bloomfield Apartments. This precautionary measure is necessary due to a shutdown associated with a line repair in the area.
Source publication date: 2021 08 31
Recent Interesting Reports
1 week ago
Over recent weeks, SafelyHQ received a surge of reports from our community citing lost and delayed packages from the US Postal Service specifically citing packages that routed through Teterboro NJ Distribution Center. The New York Post - which follows and identifies signals from our community followed up... on our story and reported on it yesterday.
If you have any health, safety, or community issue, including issues with delivery services, report it to SafelyHQ. Reporting will help identify and bring attention to common problems that impact friends, family, and our communities at the local and national level.
Read the full NY Post story here: nypost.com
USPS Teterboro & Kearny NJ Dist Centers, USPS Teterboro Distribution Center, Industrial Avenue, Teterboro, NJ, USA
5 days ago
Priority mail packages bouncing up and down the east coast unnecessarily for days, 4 days later my package is further away from being delivered than when it started. Please fire the guy running this sh*t show.
2 missing mailed packages, USPS Teterboro Distribution Center, Industrial Avenue, Teterboro, NJ, USA
1 week ago
I mailed out a Shutterfly book to my cousin in Fl, from where I live in NY on July 1st and the last known tracking of it was 4 days later in aTeterboro, NJ. It’s a bright orange package, you can’t miss! As of today Oct. 15th,... it’s still missing. In mid Sept. Shutterfly was nice enough to print a second book, which I had sent direct from Shutterfly to Fl. My cousin never got that book either. After contacting Shutterfly again, they were kind enough to send out a 3rd book, which she finally got. For the first package, I sent out, I put in a missing claim with USPS and continue to get emails saying they are still working on finding my missing package. What a joke.
October 11, 2021 – Tuffy's Pet Foods is issuing a voluntary recall of approximately 1,600 cases of Pure Vita Salmon Entree Dog Food in a Tetrapak carton following notification from the product manufacturer of potentially elevated levels of Vitamin D. No illnesses or injuries have been reported... from consumers to date.
Consuming elevated levels of vitamin D in dog food can cause adverse reactions in dogs of all sizes, including symptoms such as vomiting, loss of appetite, increased thirst, increased urination, excessive drooling, and weight loss. When ingested at excessive levels, vitamin D can lead to serious health issues in dogs including renal dysfunction. While no reports of illness or injury have been reported from consumers to date, Tuffy’s is acting out of an abundance of caution and is removing the specific lots of product listed below from distribution.
Consumers should stop feeding the product listed below to their pets immediately. Tuffy’s recommends consumers whose dogs have consumed the potentially affected product and are exhibiting any of the above-mentioned symptoms contact their veterinarian.
- Pure Vita Salmon Entrée Dog Food TetraPak (12.5 oz. per carton). UPC: 0 73893 96202 1. Lot numbers: 0629101N1 /
0901101N1. Best By dates: 29 Jun 2023 / 1 Sep 2023.
The recalled product was distributed exclusively within the United States to distributors and retail stores. The recalled product is limited to Pure Vita Salmon Entrée Dog Food in a Tetrapak carton, bearing UPC Code "0 73893 96202 1" (found on side of the carton). Products included in the recall are identified by the "Best by Dates" and “Lot Numbers” (found on the top of the carton) as listed above. No other Pure Vita dog or cat foods, or treats are affected by this announcement.
Consumers who purchased the Pure Vita Salmon Entrée dog food product subject to this voluntary recall (as identified above) are urged to return the product to their retailer for a full refund.
For consumer information or questions regarding this voluntary recall, please contact Tuffy’s Pet Foods, Inc. at (800) 525-9155 from Monday-Friday, 8:00am-5:00pm Central Time
Company name: Tuffy’s Pet Foods, Inc.
Brand name: Nutri Source
Product recalled: Pure Vita Salmon Entrée Dog Food
Reason of the recall: Elevated Levels of Vitamin D
FDA Recall date: October 12, 2021
Check the full recall details on fda.gov
1 week ago
USPS lost yet another package at their Teterboro distribution center, reporting "Processing Exception Delay" with no way to know if it will be resolved or not.
Cook Medical Transseptal Needle and Transseptal Needle Catheter - recalled due to Complaints of rust on the products, USA
6 days ago
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... 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
I paid $7.95 to send a letter via USPS Priority Mail from Short Hills, New Jersey to Arlington, VA. I mailed the item via Priority Mail on September 28, 2021 and the receipt stated it would arrive by October 1, 2021. It did not arrive until October... 9, 2021 - eleven days later! I took my receipt to the Short Hills post office and was referred to a supervisor, who told me I could not get a refund because two-day Priority Mail did not provide a "money back guarantee" if the item was delivered late.
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... 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
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... 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