Generic drugmakers Perrigo, Sanofi, Novartis' Sandoz division and Apotex have all rushed to recall the top antacid on the market today, Zantac, which has been found to contain a suspected carcinogen for years now, unbeknownst to the FDA. The carcinogen in question, NDMA, is according toHarvard...
The FDA is responsible for monitoring the recall process to ensure that it is done according to the regulations and that it adequately protects public health in a timely manner. In the United States, recalls happen quite often. Statistics from 2011 show that 9288 products were recalled. Most ...
December 19, 2024ByThe FDA Summary Company Announcement Date: December 19, 2024 …[Read More...] Magnetic Building Sticks Sets Recalled Due to Ingestion Hazard; Violation of Federal Regulations for Toy Magnets; Sold Exclusively on Amazon.com by Elongdi ...
More FDA approvalsDrugs in Development (Not yet approved) Yutrepia Yutrepia (treprostinil) is an inhaled dry powder formulation of treprostinil tentatively approved for the treatment of pulmonary arterial... More drugs in developmentDrug Information A to Z Drug List Treatment Options Drugs by ...
Recalls of spices due to bacterial contamination monitored by the U.S. Food and Drug Administration: the predominance of Salmonellae. During the study period, the FDA monitored 21 recalls involving 12 spice types contaminated with bacterial pathogens; in all but one instance, the recalled... V ...
discovered the residue in its supplies. It attributed the impurity to a new manufacturing process it recently adopted.The FDA said it is currently investigating the levels of NDMA in the recalled products, assessing the effect on patients and working with Huahai to solve the problem in future ...
Edge Pharma, LLC is notifying its customers by email, Media and FDA alerts, and direct outreach. Consumers and institutions that have Edge Pharma, LLC products should stop using the products immediately and may either return or discard the recalled lots. Consumers with questions regarding this reca...
Pfizer has recalled all presentations of Chantix. More information on the recall can be found at https://www.fda.gov/drugs/drug-safety-and-availability/fda-updates-and-press-announcements-nitrosamine-varenicline-chantix.[1] The generic presentations are not affected by this shortage. Available ...
FDA Recall The FDA issued a recall of Baycol® in August 2001 due to the deaths of 30 people who developed rhabdomyolysis and eventual kidney failure while taking the cholesterol drug. Baycol® is the only statin drug that has been recalled by the FDA. ...
Supplements were purchased a mean (SD) of 34.3 (11.5) months after the FDA recall (range, 8-52 months). Seventy-four percent of supplements (20/27) were produced by US manufacturers. One or more pharmaceutical adulterant was identified in 66.7% of recalled supplements still available for ...