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Applebee's Grill + Bar, 5605 2nd Ave, Kearney, NE 68847, USA
Total all time reports:
1
Latest report: July 5, 2020 12:00 PM
More incidents from:
Bar
Restaurant
Coronavirus - Covid-19
Applebee's
5605, 2nd Avenue
Kearney
Nebraska
United States
Employee test positive for Covid-19
July 5, 2020 12:00 PM
“An Applebee's worker at the 5605 Second Ave. location contracted COVID-19. The team member worked on June 21/
Source: kearneyhub.com See Less”
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August 3, 2021 12:02 AM
“Company name: Je Dois L’avoir Boutique
Brand name: 365 Skinny
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Reason of the recall: Product contains sibutramine
FDA Recall date: August 02, 2021
Recall details: Hanford, California, Je Dois L’avoir Boutique is voluntarily recalling all of the 365 Skinny... See More High Intensity Pills and or 365 Skinny Emergency Boutique, 30 day capsules supply to the retail/consumer level. The 365 Skinny High Intensity Pills and 365 Skinny Emergency Boutique have been found to contain Sibutramine which is a controlled substance by the DEA and poses significant health risks to consumers both products are from the same manufacturer 365 Skinny is the strongest form and the 365 Skinny Emergency is for people with high blood pressure, diabetes but not limited to other chronic illnesses.
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The product is used together with diet and exercise to assist with weight loss and is packaged in bottles of 30 capsules 600mg per capsule. All lots and expiration dates of any of these products are being recalled. Je Dois L’avoir is recalling ALL 365 Skinny High Intensity Pills and 365 Emergency Boutique that it has sold to the public as seen below. Je Dois L’avoir is notifying its distributors and customers by email and is arranging for return/replacement etc. of all recalled products. Consumers that have 365 High Intensity Skinny or 365 Skinny Emergency Boutique which is being recalled should stop using/return to place of purchase/discard/contact Je Dois L’avoir Boutique Immediately.
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July 14, 2021 9:01 PM
“Company name: Johnson& Johnson
Brand name: Neutrogena, Aveeno
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Recall details: Johnson & Johnson Consumer Inc. (JJCI) is voluntarily recalling all lots of five NEUTROGENA® and AVEENO® aerosol sunscreen... See More product lines to the consumer level. Internal testing identified low levels of benzene in some samples of the products. Consumers should stop using the affected products and follow the instructions set forth below.
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The recalled sunscreen products are packaged in aerosol cans. The products were distributed nationwide through a variety of retail channels.
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Check the full recall details on fda.gov
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July 19, 2021 9:02 PM
“Company name: Alpha Male Plus
Brand name: Alpha Male Plus
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Reason of the recall: Undeclared Tadalafil
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Risk Statement: Consumers with underlying medical conditions who take Alpha Male Plus Male Enhancer with undeclared tadalafil may experience serious health risks. For example, PDE-5 inhibitors may interact with nitrates found in some prescription drugs (such as nitroglycerin) lowering blood pressure to dangerous levels that may be life-threatening. Consumers with diabetes, high blood pressure, or heart disease often take nitrates. To date, Alpha Male Plus has not received any reports of adverse events related to this recall.
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This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Check the full recall details on fda.gov
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Chantix is a treatment to help patients quit smoking and is intended for short term use. People who smoke cigarettes are 15 to 30 times more likely to get lung cancer than people who do not smoke. Smoking is also associated with many other cancers. CHANTIX has a safety profile that has been established over 15 years of marketing authorization and through a robust clinical program. Pfizer believes the benefit/risk profile of CHANTIX remains positive. Patients currently taking Chantix should consult with their doctor to confirm if they received an affected lot, and if appropriate, about alternative treatment options.
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The product lots were distributed nationwide to wholesalers and Distributors in the United States and Puerto Rico from June 2019 to June 2021.
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July 23, 2021 12:03 AM
“Company name: HIS
Brand name: HIS
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Reason of the recall: Undeclared Sibutramine
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Sibutramine was an FDA-approved drug used as an appetite suppressant for weight loss but was withdrawn from the market because of safety issues. The presence of sibutramine in Miss Slim renders it an unapproved drug for which safety and efficacy has not been established and therefore subject to a recall. To date, HIS has not received any reports of adverse events related to this recall.
The product is marketed as a dietary supplement and is packaged 10 count UPC (742137605030) and 30 count UPC (609728434472) capsules. The product sold online at missslimusa.com.
Risk Statement: Products containing sibutramine pose a threat to consumers because sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias or stroke.
HIS is notifying its customers by website missslimusa.com and is arranging for return of all recalled products. Consumers that have Miss Slim which is being recalled should stop using it. 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.
Check the full recall details on fda.gov
Source: FDA See Less”
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