Taco Bell, 1126 W 7th St, Auburn, IN 46706, USA

1. Employees are exposed to health hazards in that the employer is allowing employees who have tested positive for COVID-19 to work with symptoms of the virus, such as fever.

Alleged Hazards: 1, Employees Exposed: 10
Source: Osha.gov | Receipt Date: 2021-08-25 See Less

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1. The employer is not taking action to slow the spread of Covid-19 in the workplace.

Alleged Hazards: 1, Employees Exposed: 25
Source: Osha.gov | Receipt Date: 2021-08-09 See Less

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They making employees who have tested positive for COVID-19 work. Employees are made to work after exposure to COVID-19 and while they are sick and showing symptoms. Employees are told to not inform others. The guidelines state that if they test positive, employees are being required to... See More return to work in three days. They are requiring employees to return to work even if they test positive before three days. Employees are told if they are showing symptoms or exposed and choose to be tested, that is their choice, but they are still required to come to work. They are telling employees that they have to come to work even if they have symptoms or if they have tested positive, as long as they are wearing a mask. They are not enforcing that employees wear masks, they are only giving employees cloth masks, employees are taking off their masks.


Source: Osha.gov | Receipt Date: 2020-07-29 See Less

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'- Not providing hand sanitizer. - No disinfecting being done in the facility.


Source: Osha.gov | Receipt Date: 2020-08-07 See Less

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5199(c): Outbreak at jail since June. 39 inmates who have gotten infected in the H Tank. 5199(c): Jail made a decision to not isolate inmates. 5199(c): Jail transported inmates from the infected area to North Kern State Prison. Inmates were tested prior to departure from the jail.... See More Inmates tested negative; however, upon arrival to the prison, the inmates tested positive for the delta strain.

Alleged Hazards: 3, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-07-06 See Less

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1) The employer does not have a Heat Stress Program and train employees on the systems, hydration procedures and cool down procedures to follow. 2) Employees are exposed to health hazards from the COVID-19 virus in that the employer does not require employees to social distance per... See More CDC (Center for Disease Control and Prevention) guidelines. Areas such as but not limited to the city carriers work due to not having staggered work hours. 3) Employees are exposed to health hazards associated with COVID-19 in that the employer does not require/enforce employees to wear masks per CDC (Center for Disease Control and Prevention) guidelines. 4) Employees are exposed to health hazards related to the employer not informing them of when other two employees have tested positive for COVID-19 (coronavirus disease) within the facility as in accordance to CDC (Center for Disease Control and Prevention) guidelines. 5) Employees are exposed to health hazards related to the employer not cleaning and sanitizing the workplace regularly per CDC (Center for Disease Control and Prevention) guidelines after employees tested positive for COVID-19. 6) Employees are exposed to health hazards associated with COVID-19 in that the employer does not screen employees for symptoms of the virus per CDC (Center for Disease Control and Prevention) guidelines. 7) Employees are running out of soap/hand towels in the bathroom area. 8) Proper sanitation is not being maintained due to trash overflowing and proper general cleaning in common areas due to no custodian service.


Source: Osha.gov | Receipt Date: 2021-07-29 See Less

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3205(c)(6)(A): Employer is not enforcing face covering for non-vaccinated employees.

Alleged Hazards: 1, Employees Exposed: 1
Source: Osha.gov | Receipt Date: 2021-06-25 See Less

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1. The employer failed to inform employees that they have worked with children who were sick and tested positive with COVID-19 (coronavirus disease) within the facility as in accordance to CDC (Center for Disease Control and Prevention) guidelines. 2. The employer failed to ensure periodic cleaning of... See More the facility in accordance to CDC (Center for Disease Control and Prevention) guidelines for the COVID-19 pandemic.

Alleged Hazards: 3, Employees Exposed: 30
Source: Osha.gov | Receipt Date: 2021-07-21 See Less

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Weeks-long lane closures are expected to begin Monday along South Gay Street between Woodfield Drive and Reese Avenue in Auburn. The city says some residences in the area will experience a power outage during this time. Affected customers will be notified by Alabama Power.

Source: wtvm.com See Less

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Strong storms that moved through the region Thursday afternoon knocked out power for more than 1,000 customers in Cayuga County.

As of 4:45 p.m., Rochester Gas and Electric reported 1,007 customers without power in Cato, Meridian and Ira. RG&E estimated that most customers would have their power... See More restored by 7:45 p.m. Power appeared to have been restored to all Cayuga County customers before 7:30 p.m.

Source: auburnpub.com See Less

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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

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It’s been over 20 days for next-state packages and still have not arrived. See Less

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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

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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

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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

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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

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Bronx. Wagon a package saying in transit since Saturday from teterboro  See Less

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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

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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

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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

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