Binax now recall
WebMar 28, 2007 · Binax, Inc. dba IMPD 10 Southgate Rd Scarborough ME 04074-8303: For Additional Information Contact: Jenny Fuchs 207-730-5700 Manufacturer Reason for Recall: Tip of the foam swab could detach from the shaft causing injury to the patient. FDA Determined Cause 2: Other: Action: Inverness Medical issued recall notification by letter … 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 …
Binax now recall
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WebSep 21, 2024 · The FDA urged clinical laboratories and healthcare providers to retest any patients who have recently received a positive result from two of Abbott’s PCR COVID-19 assays after identifying a... 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 …
WebJan 11, 2024 · The Abbott BinaxNOW, a widely used at-home coronavirus test, can detect most people who are infected with the new Omicron variant and are carrying high levels of the virus, according to a new ... WebBINAX NOW RSV TEST, MODEL 430-000 AND BINAX NOW NASOPHARYNGEAL SWAB ACCESSORY PACK, MODEL 400-065: Applicant: BINAX, INC. 217 READ ST. PORTLAND, ME 04103 Applicant Contact: PAMELA ANGELL: ... Recalls: CDRH Recalls - - Links on this page: Page Last Updated: 04/03/2024.
WebFeb 9, 2024 · SD Biosensor, Inc., a global in-vitro diagnostics company, voluntarily recalled their STANDARD Q COVID-19 Ag Home Test on January 31. The tests were reportedly illegally imported into the US, … WebThe BinaxNOW COVID-19 Ag Card Home Test is authorized for prescription use at home with self-collected nasal swab samples from individuals ages 15 years or older who are …
WebMar 28, 2007 · Recall Number: Z-0826-2007: Recall Event ID: 37843: Product Classification: Influenza A&B Test Kit - Product Code GNX: Product: BinaxNOW A&B Kit 10 Test Kit (Japan) Part No. 416-110J contains NP Swabs with '8995' labeled on the swab wrapper: Code Information: Lot number: 24162: Recalling Firm/ Manufacturer: Binax, …
WebJan 28, 2024 · Virus was recovered from 96 (35.0%) of 274 analyzed specimens that were positive by either test, including 85 (57.8%) of 147 with concordant positive results and … csl walthamWebApr 6, 2024 · April 7, 2024 Consumer Information: iCAST Covered Stent System – P120003 (Atrium Medical Corporation) Class I Recall: Philips Respironics Recalls Certain Reworked DreamStation CPAP, BiPAP... csl warrantsWebNov 8, 2024 · The Ellume Recall On December 15, 2024, the Ellume COVID-19 Home Test became the first fully at-home SARS-CoV-2 testing kit to receive EUA for over-the … csl warner robinsWebMar 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 … eagles christmas ornamentsWebApr 19, 2024 · The BinaxNOW COVID-19 Ag 2 Card is a lateral flow immunoassay intended for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2 in direct anterior nasal (nares) swab samples … cslw6b200mcsl wargamesWebMar 28, 2007 · Binax, Inc. dba IMPD 10 Southgate Rd Scarborough ME 04074-8303: For Additional Information Contact: Jenny Fuchs 207-730-5700 Manufacturer Reason for … csl warr acres