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Harper's Restaurant & Brewpub, 131 Albert St, East Lansing, MI 48823, United States
Latest report: July 1, 2020 12:00 PM
YL
Covid-19 Outbreak linked to restaurant
3 years ago
Harper’s Restaurant and Brewpub in East Lansing is linked to at least 85 positive cases of the coronavirus and patrons are being asked to take self-quarantine measures.
Source: krmg.com See Less
196
WJ
14 people that visited have test positive for Covid-19
3 years ago
14 people have tested positive for COVID-19 after recently visiting Harper's Restaurant & Brewpub in downtown East Lansing. If you visited between June 12 - June 20 to watch for symptoms.
Source: fox47news.com See Less
196
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Detect, Inc. Over the counter Covid-19 Test - recalled due to may give false negative results, USA
11 months ago
Detect, Inc. is voluntarily recalling specific lots of the Detect Covid-19 Test™, their molecular, over-the-counter test used to identify SARS-CoV-2 (the virus that causes Covid-19) in self-collected nasal swabs. The recall affects a total of 11,102 tests shipped to customers from July 26th, 2022 through August 26th,... See More 2022. The test was granted Emergency Use Authorization (EUA) from the U.S. Food and Drug Administration (FDA) on October 28, 2021. To date, Detect has not received any reports of false negative results related to the affected lots and is issuing this recall out of an abundance of caution.
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There is an increased chance that the tests from the lot numbers listed below may give false negative results. Detect has conducted a thorough investigation to identify this issue and has made the decision to conduct a voluntary recall for these lots. To date, Detect has not received any reports of false negative results related to the affected lots and is issuing this recall out of an abundance of caution. The reliability of positive test results is not affected.
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Detect, Inc. will issue a refund* for the affected tests (as verified by Detect) upon customers’ acknowledgement of receipt of the recall-related communication and confirmation that any affected tests in possession have been disposed of.
Company name: Detect, Inc.
Brand name: Detect
Product recalled: Over the counter Covid-19 Test
Reason of the recall: There is an increased chance that the tests from the lot numbers listed below may give false negative results
FDA Recall date: December 12, 2022
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LEADER OTC Ophthalmic Sterile Drops - recalled due to Insanitary manufacturing conditions, USA
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Cardinal Health, Inc. is initiating a voluntarily recall for all lots of ophthalmic products supplied by Velocity Pharma, LLC to the consumer level. Cardinal Health, Inc. received information from FDA indicating investigators found insanitary conditions in the manufacturing facility and positive bacterial test results from environmental sampling... See More of critical drug production areas in the facility. Products were distributed Nationwide to Wholesalers and Retailers starting December 12, 2021. To date, Cardinal Health, Inc., and its subsidiaries have received reports of three (3) adverse events related to these products. The reports of adverse events were shared with their supplier, Velocity Pharma, LLC.
The recalled products are:
- LEADER™ Eye Irritation Relief (Polyvinyl Alcohol, 0.5%, Povidone, 0.6%, and Tetrahydrozoline Hydrochloride, 0.05%), 0.5 FL OZ bottle (15 mL), NDC:
- LEADER™ Dry Eye Relief (Carboxymethylcellulose Sodium, 1%), 0.5 FL OZ bottle (15 mL), NDC: 70000-0089-1
- LEADER™ Lubricant Eye Drops (Carboxymethylcellulose Sodium, 0.5%), 0.5 FL OZ bottle (15 mL). NDC: 70000-0090-1
- LEADER™ Lubricant Eye Drops (Carboxymethylcellulose Sodium, 0.5%), 2 bottles, 0.5 FL OZ (15 mL) each. NDC: 70000-0090-2 (Carton) 70000-0090-1 (Bottle)
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Risk Statement: For those patients who use these products, there is a potential risk of eye infections that could result in partial vision loss or blindness. These products are intended to be sterile. Ophthalmic drug products pose a potential heightened risk of harm to users because drug applied to the eyes bypass some of the body’s natural defenses.
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TING® 2% Miconazole Nitrate Athlete’s Foot Spray Antifungal Spray Powder is packaged in green and white aerosol cans with Lot codes located on the bottom of the can.
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