Philips Agrees to Stop Selling CPAP Machines as Part of Settlement Deal Dangerous Drugs AstraZeneca Agrees to $425 Million for PPI Lawsuits[...] Dangerous Drugs GSK Settles First Zantac Cancer Lawsuit[...] Have you been affected by a drug or device listed?
June 13, 2024 — The U.S. Food and Drug Administration (FDA) announced that Teleflex, and their subsidiary Arrow International, are recalling the Arrow FiberOptix Intra-Aortic Balloon Catheter Kit and ... FDA Announces Abbott Recall of HeartMate 3 Left Ventricular Assist System (LVAS) Implant ...
. FDA provides update on its ongoing investigation into ARB drug products; reports on finding of a new nitrosamine impurity in certain lots of losartan and product recall. Retrieved fromhttps://www.fda.gov/news-events/press-announcements/fda-provides-update-its-ongoing-investigation-arb-drug-...
FDA Seeking Legal Action In Drug RecallMalcolm Gladwell
Current recall notices published by the Food and Drug Administration (FDA) indicate that impacted COVID-19 tests must be disposed of immediately, as bacterial organisms like Enterococcus, Enterobacter, Serratia species and Klebsiella potentially have contaminated materials. While the agency has yet to ...
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 ...
Contrary to what most people think, just because a drug or device is FDA-approved, it does not mean the product is guaranteed to be safe. In fact,manufacturers recallabout 4,500 drugs and medical devices annually. While the FDA has efforts in place to minimize these safety risks, there ar...
Other groups, such as the Alzheimer’s Association, have supported the drug’s approval. The Alzheimer’s Association‘s website stated on Friday, “This is a critical time, regardless of the FDA’s final judgment. We’ve never been this close to approving an Alzheimer’s drug that could ...
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration. Source: FDA Acetaminophen Tablets by Medline Industries: Recall - Mislabeling with Incorrect Strength Oct 15, 2015 | Audience: Pharmacy, Consumer
FDA has the power to recall products on the market, if necessary, for safety and other reasons. Understanding the Food and Drug Administration (FDA) The Food and Drug Administration is the federal government agency assigned to protect and promote public health. This is done by assessing and ass...