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Voluntary Recall of Three Detect Covid-19 Test Lots
… ket-withdrawals-safety-alerts/voluntary-recall-three-detect-covid-19-test-lots … Detect, Inc. is voluntarily recalling specific lots of the Detect Covid-19 Test™, our molecular, over-the-counter test used to …
SD BIOSENSOR, Issues Notification of Voluntary Recall of ‘STANDARD Q COVID-19 Ag Home Test’
… d-biosensor-issues-notification-voluntary-recall-standard-q-covid-19-ag-home-test … January 31, 2022. SD Biosensor, Inc., a … company, is voluntarily recalling its STANDARD Q COVID-19 Ag Home Test in the United States, due to confirmed …
Recall Notice - SD Biosensor, Inc. Requests Discontinuation of Use and Disposal of Specific Pilot™ COVID-19 At-Home Tests in the United States Due to Microbial Contamination in the Liquid Buffer Solution
… -requests-discontinuation-use-and-disposal-specific-pilottm-covid-19 … SEOUL, South Korea, May 4, 2023 /PRNewswire/ -- SD … that consumers stop using and dispose of specific Pilot COVID-19 At-Home Tests in the United States because …
ACON Laboratories Issues a Recall of Non-EUA Authorized “Flowflex™ SARS-CoV-2 Antigen Rapid Test (Self-Testing)” Tests From the U.S. Market
… Laboratories”), the legal manufacturer of the “ Flowflex ™ COVID-19 Antigen Home Test ” (FDA Emergency Use Authorization … cleared, or authorized by the FDA. The “ Flowflex COVID-19 Antigen Home Test” cannot be legally imported, …
Urgent Notice of Product Recall
… claims that the product will prevent, treat, or cure COVID-19. It is the government's position that consumers who use … claims that the product will prevent, treat, or cure COVID-19. It is the government's position that consumers who …
CME America Provides Update on Two Previously Announced Voluntary Recalls Related to Ambulatory Infusion Pumps and Sets
… access to critical medical equipment, particularly as the COVID-19 pandemic continues to evolve in the United States, CME … clinical disruption and maintain patient focus during the COVID-19 pandemic: Use of products in the field in accordance …
The J. M. Smucker Co. Issues Voluntary Recall of Select Jif® Products Sold in the U.S. for Potential Salmonella Contamination
… products, including product recalls; the impact of the COVID-19 pandemic on our business, industry, suppliers, customers, … conditions, natural disasters, pandemics (including the COVID-19 pandemic), or other calamities; risks related to the …
Gilead Issues A Voluntary Nationwide Recall of Two Lots of Veklury® (Remdesivir) Due to Presence of Glass Particulates
… old and weighing ≥40 kg requiring hospitalization for COVID-19. The lyophilized form of Veklury (remdesivir 100 mg for …
CME America Announces a Follow-Up on the Voluntary Recall of BodyGuard® Infusion System Administration Sets
… will continue to maintain continuity of care during the COVID-19 pandemic. Until such time that the BodyGuard® pumps have …
Sunstar Americas Inc. Expands Voluntary Nationwide Recall of Paroex® Chlorhexidine Gluconate Oral Rinse USP, 0.12% Due to Microbial Contamination
… respiratory conditions, including those infected with Covid-19, is particularly unsafe. The prescription oral rinse …
Sandoz, Inc. Issues Nationwide Recall of One Lot of Enoxaparin Sodium Injection, USP 40mg/0.4 mL Due to Temperature Excursion During Shipping
… of and efforts to mitigate pandemic diseases such as COVID-19; safety, quality, data integrity or manufacturing issues; …
Novartis Issues Voluntary Nationwide Recall of One Lot of Sandimmune® Oral Solution (Cyclosporine Oral Solution, USP), 100 mg/mL Due to Crystallization
… of and efforts to mitigate pandemic diseases such as COVID-19; safety, quality, data integrity or manufacturing issues; …