Last week, the FDA added two more eye drops to its recall list:Apotex Corp Brimonidine Tartrate Ophthalmic Solution (0.15%)andPharmedica USA LLC Purely Soothing 15% MSM Drops. These recalls follow a recall on batches of artificial tears in early February 2023. Each...
2022 FDA Drug Approval List, 2022 Biological Approvals and Approved Cellular and Gene Therapy Products Posted in cell-based therapy, Drug Discovery Chemistry, FDA, FDA, CE Mark & Global Regulatory Affairs: process management and strategic planning - GCP, GLP, ISO 14155, Pharmaceutical Discovery, ...
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 ...
July 21, 2022 -- Family Dollar is initiating a voluntary retail level product recall of certain products regulated by the U.S. Food and Drug Administration (FDA) that were stored and inadvertently shipped to certain stores on or around May 1, 2022 through June 10, 2022 due to product being...
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration. STERILE PRODUCTSNDC ALUMINUM POTASSIUM SULFATE CONCENTRATED (PF) 300 G/300 ML 05446-0637-03 BUFFERED LIDOCAINE HCL (PF) 1% 05446-0850-10 BUFFERED LIDOCAINE HCL / EPINEPHRINE SOLUTION (PF) 1% / 1:100...
WARNING LETTERCMS 535005December 19, 2017VIA UPS NEXT DAY AIRPaul F. Devine, CEOPresidentC.O. Truxton, Inc.136 Harding A
On October 26, 2021, you, and Virgin Scent Inc., issued a voluntary nationwide recall of two batches of artnaturals SCENT FREE HAND SANITIZER due to the presence of benzene, acetaldehyde, and acetal impurities. On April 22, 2022, the scope of the recall of artnaturals SCENT FREE HAND SANIT...
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 ...
U.S. Food and Drug Administration. (2019, March 1). 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-...
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...