Flowflex rapid test recall
WebThe Flowflex SARS-CoV-2 Rapid Antigen Test is the first in this family of lateral flow testing products. View Product. ... Since the launch of its Flowflex COVID-19 Antigen Home Test, ACON Laboratories, Inc. has continued testing for product stability to extend the shelf-life. These results have been shared with the FDA. WebPeople should avoid certain ACON Laboratories' Flowflex SARS-CoV-2 Antigen Rapid Test (Self-Testing) tests, specifically those that are packaged in a dark blue box, the FDA said. It also warned ...
Flowflex rapid test recall
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WebAn official website of the United States government, Recalls, Market Withdrawals and Safety Alerts, Do Not Use Certain ACON Flowflex COVID-19 Tests: FDA Safety Communication, report the problem through the MedWatch Voluntary Reporting Form, Report any problems you experience with the Flowflex SARS-CoV-2 Antigen Rapid … WebMar 16, 2024 · The one to avoid -- which was recalled on January 9-- is the "Flowflex SARS-CoV-2 Antigen Rapid Test (Self-Testing)." ACON said in its recall notice that it is an "unauthorized, adulterated and ...
WebMar 16, 2024 · The one to avoid -- which was recalled on January 9-- is the "Flowflex SARS-CoV-2 Antigen Rapid Test (Self-Testing)." ACON said in its recall notice that it is an "unauthorized, adulterated and ... http://publichealth.lacounty.gov/acd/ncorona2024/covidtests/self/
WebMar 16, 2024 · LAS VEGAS (KLAS) — The state of Nevada announced on Tuesday that the Flowflex\COVID-19 Antigen home tests ordered for the state are not affected by the … WebMar 18, 2024 · This recall shall have no impact on the distribution and use of the CE marked “Flowflex SARS-CoV-2 Antigen Rapid Test (Self-Testing)” in Europe and other markets outside of the U.S. This recall shall have no impact on the distribution and use of the FDA authorized “Flowflex COVID-19 Antigen Home Test” in the United States.
WebJan 9, 2024 · Recall Status 1: Open 3, Classified: Recall Number: Z-0945-2024: Recall Event ID: 89755: Product Classification: Coronavirus antigen detection test system. - …
WebOct 5, 2024 · The agency expects the ACON Laboratories Flowflex COVID-19 Home Test to double the nation’s rapid at-home testing capacity over the next several weeks. The … describe training experienceWebJan 19, 2024 · Approximately 200,100 Flowflex SARS-COV-2 Antigen Rapid Tests (Self-Testing) have been recalled by the Food and Drug Administration (FDA) as the tests were never granted approval by the agency. In a recall notice, the FDA says the tests have not been authorized for emergency use to test for COVID-19 and “cannot be determined to … chsbooking.fhs.gov hkWebJan 14, 2024 · COVID-19: Recall Issued For Free Self-Testing Kits. Orange County’s Department of General Services has announced that the Flowflex antigen rapid test kits the county distributed to residents have been recalled by the manufacturer. The kits were distributed to residents on Thursday, Jan. 13 in the Towns of Wallkill and New Windsor, … chs boomWebMar 11, 2024 · ACON Laboratories Issues a Recall of Non-EUA Authorized “Flowflex™ SARS-CoV-2 Antigen Rapid Test (Self-Testing)” Tests From the U.S. Market For Immediate Release March 11, 2024 Contact Information ACON Laboratories Customer Support 1-800-838-9502 [email protected] Company Announcement … describe tracking as a data collection methodWebJan 14, 2024 · The Food and Drug Administration issued a recall late last month for “Flowflex SARS-CoV-2 Antigen Rapid Test (Self-Testing)," a product sold at an unknown number of pharmacies and distributed by ... chs booking fhs gov hkWebJan 19, 2024 · Approximately 200,100 Flowflex SARS-COV-2 Antigen Rapid Tests (Self-Testing) have been recalled by the Food and Drug Administration (FDA) as the tests … chs booking fhsWebJan 14, 2024 · The Food and Drug Administration issued a recall late last month for “Flowflex SARS-CoV-2 Antigen Rapid Test (Self-Testing)," a product sold at an unknown number of pharmacies and distributed by ... chs boot