WebMar 28, 2007 · Class 2 Device Recall BinaxNOW. Kit Lot Numbers: 023437, 024056, 024057, 024436, 024516, 024518, 024694, 024695, 024882, 025090, 025089 NP Swabs Lot Number: 8995. Tip of the foam swab could detach from the shaft causing injury to the patient. Inverness Medical issued recall notification by letter on 3/28/07. Customers are … WebThe BinaxNOW™ COVID-19 Ag Card has been designed to minimize the likelihood of false positive test results. However, in the event of a false positive result, risks could include the
Covid-19 At Home Tests Recalled for False Positives
WebNov 8, 2024 · On October 5, Ellume recalled 200,000 of the test kits shipped to US retailers from April through August due to concerns that they were reporting a higher than … WebRecall of Device Recall BinaxNOW Manufacturer Binax, Inc. dba IMPD Manufacturer Address Binax, Inc. dba IMPD, 10 Southgate Rd, Scarborough ME 04074-8303 Source USFDA 4 devices with a similar name Learn more about the data here Device Recall BinaxNOW Model / Serial Kit lot Numbers: 023357, 023566, 024629, 024631, Product … chuck e cheese buffet commercial
FDA alerts providers to COVID-19 rapid test recall AHA …
WebAug 21, 2024 · The BinaxNOW antigen test, which can provide COVID-19 results within 15 minutes, was popular earlier in the pandemic as a way for people to quickly learn … WebFeb 9, 2024 · The Food and Drug Administration ( FDA) announced a recall of the STANDARD Q COVID-19 Ag Home Test because of its illegal importation to the United … WebOct 15, 2024 · Text Size. Abbott has recalled two of its Alinity COVID-19 test kits after finding they can yield false positive results. Abbott is recalling its Alinity m SARS-CoV-2 AMP kit and Alinity m Resp-4 ... design liability in construction contracts