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17 individuals tested positive for Covid-19, Manatee County School District, FL, USA

3 years ago

Florida, United States

17 individuals at Manatee schools have recently tested positive for COVID-19. The cases include: one student at Bayshore Elementary School, one student at Bayshore High School, one employee at Braden River Elementary School, one student at Braden River High School one student at Braden River Middle School, one employee and one student at Manatee High School, one student at Miller Elementary School, one student at Nolan Middle School, one student at Oneco Elementary School, one student at Palm View K-8 School, Three students at Palmetto, one student at Parrish Community High School, and one employee at Rogers-Garden Bullock Elementary School.

Source: bradenton.com

177


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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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Lot Number: HY263, Use By Date: 1/1/2023, Number of Tests Shipped: 1,800
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Test users who attempt to use recalled tests will be notified in the Detect App™ that the test has been recalled and may not be used.

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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