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McDonald's, 4200 South St, Lafayette, IN 47905, United States
Total all time reports:
1
Latest report: May 17, 2020 12:00 PM
More incidents from:
Cafe
Restaurant
Coronavirus - Covid-19
McDonald's
4200, South Street
Lafayette
Indiana
United States
McDonald's employee contracted coronavirus
May 17, 2020 12:00 PM
“A McDonald’s restaurant in Lafayette near Interstate 65 remained closed this week after the company said employees tested positive for coronavirus. If you visited the restaurant location during that time, please report it and any other location that you visited.
Source: jconline.com See Less”
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“Company name: Je Dois L’avoir Boutique
Brand name: 365 Skinny
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July 14, 2021 9:01 PM
“Company name: Johnson& Johnson
Brand name: Neutrogena, Aveeno
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Reason of the recall: Testing identified low levels of benzene
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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
Source: FDA See Less”
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“Company name: Alpha Male Plus
Brand name: Alpha Male Plus
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Reason of the recall: Undeclared Tadalafil
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Recall details: Tucson, AZ, Alpha Male Plus is voluntarily recalling all lots within expiry of Alpha... See More Male Plus Male Enhancer fruit chews to the consumer level. FDA analysis has found the product to be tainted with tadalafil, an ingredient known as a phosphodiesterase (PDE-5) inhibitor found in a FDA approved product for the treatment of male erectile dysfunction. The presence of tadalafil in Alpha Male Plus Male Enhancer renders the product an unapproved drug for which safety and efficacy have not been established and, therefore, subject to recall.
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Alpha Male Plus was marketed as a dietary supplement for male sexual enhancement and is packaged in 1strip per foil pouch within a cardboard box, UPC [8 60003 03770 6] [8 60003 74512 0].
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Check the full recall details on fda.gov
Source: FDA See Less”
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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.
For more recall details including the NDC, Lot Number, Expiration Date, and Configuration details for Chantix Tablets check: fda.gov
Source: FDA See Less”
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July 23, 2021 12:03 AM
“Company name: HIS
Brand name: HIS
Product recalled: Dietary Supplement for Weight Loss
Reason of the recall: Undeclared Sibutramine
FDA Recall date: July 22, 2021
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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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