The Food and Drug Administration (FDA) has to recall (召回) hundreds of foods every year. Like cookie snack packs with pieces of blue plastic hiding inside, dressing and sauce containing salmonella (沙门氏菌) or various jams containing with lead (铅). It can take a few months before a ...
FDA. (2023, March 1). FDA Updates and Press Announcements on Angiotensin II Receptor Blocker (ARB) Recalls (Valsartan, Losartan, and Irbesartan). Retrieved fromhttps://www.fda.gov/drugs/drug-safety-and-availability/fda-updates-and-press-announcements-angiotensin-ii-receptor-blocker-arb-recalls-val...
FDA will require that a warning be added to the labels of prescription drug products containing acetaminophen to address the risk of serious skin reactions. FDA will also request that manufacturers add a warning about serious skin reactions to the product labels of OTC acetaminophen drug products ma...
Food and Drug Administration. Source: FDA Hospira, Inc. Issues a Voluntary Nationwide Recall for Sodium Bicarbonate Injection and Lidocaine HCl Injection Due to the Potential for Presence of Glass Particulate MatterOct 2, 2023 | Audience: Health Professional, Pharmacy, Consumer October 2, 2023 - ...
2022 FDA Drug Approval List, 2022 Biological Approvals and Approved Cellular and Gene Therapy Products Reporter: Aviva Lev-Ari, PhD, RN SOURCE Tal Bahar’s post on LinkedIn on 1/17/2023 Novel Drug Approvals for 2022 FDA’s Center for Drug Evaluation and Research (CDER) New Molecular Entitie...
The FDA identified it as the most serious type of recall, though, as it may cause serious injury or death. Boston Scientific updated […] Filed Under: Cardiovascular, Catheters, Food & Drug Administration (FDA), Pulsed-Field Ablation (PFA), Recalls, Regulatory/Compliance Tagged With: Boston ...
The Food and Drug Administration warned Wednesday of another imported eye product that could be contaminated with bacteria, in the wake of an outbreak earlier this year of highly drug-resistant bacteria that hospitalized and blinded some patients. ...
Nov 17, 2023 Another eye drop recall pulls 28 products from store shelves Kilitch Healthcare India is recalling the products more than three weeks after the FDA warned against their use. Nov 17, 2023 FDA approves new weight loss drug Zepbound ...
FDA Announces Teleflex/Arrow International Recall Arrow FiberOptix and UltraFlex Intra-Aortic Balloon (IAB) Catheter Kits June 13, 2024 — TheU.S. Food and Drug Administration(FDA) announced thatTeleflex, and their subsidiaryArrow... June 13, 2024 ...
FDA Seeking Legal Action In Drug RecallMalcolm Gladwell