Urgent Voluntary Recall: CorneaGen Cornea/ Cornea Patch Grafts; CorneaGen is voluntarily recalling Corneal Patch Grafts bearing the following product numbers: W419221004861104; W419221004861105; W419221004861106; W419221004861103
2022 Biologics Recalls
http://www.fda.gov/vaccines-blood-biologics/recalls-biologics/2022-biologics-recalls
FDA Flexibilities to Yield Millions of Cans of Additional Infant Formula in Coming Months to Increase Supply Available to U.S. Consumers
FDA Flexibilities to Yield Millions of Cans of Additional Infant Formula in Coming Months to Increase Supply Available to U.S. Consumers
http://www.fda.gov/news-events/press-announcements/fda-flexibilities-yield-millions-cans-additional-infant-formula-coming-months-increase-supply
FDA Roundup: May 24, 2022
FDA Roundup: May 24, 2022
http://www.fda.gov/news-events/press-announcements/fda-roundup-may-24-2022
Teva Issues Voluntary Nationwide Recall of One Lot of Anagrelide Capsules, USP 0.5 mg Due to Dissolution Test Failure
FDA Approves First Treatment for Eosinophilic Esophagitis, a Chronic Immune Disorder
FDA Approves First Treatment for Eosinophilic Esophagitis, a Chronic Immune Disorder
http://www.fda.gov/news-events/press-announcements/fda-approves-first-treatment-eosinophilic-esophagitis-chronic-immune-disorder
FDA Roundup: May 20, 2022
FDA Roundup: May 20, 2022
http://www.fda.gov/news-events/press-announcements/fda-roundup-may-20-2022
FDA Urges Drug Manufacturers to Develop Risk Management Plans to Promote a Stronger, Resilient Drug Supply Chain
FDA Urges Drug Manufacturers to Develop Risk Management Plans to Promote a Stronger, Resilient Drug Supply Chain
http://www.fda.gov/news-events/press-announcements/fda-urges-drug-manufacturers-develop-risk-management-plans-promote-stronger-resilient-drug-supply
New FDA Draft Guidance Aims to Increase Safety Information About Dietary Supplement Marketplace
New FDA Draft Guidance Aims to Increase Safety Information About Dietary Supplement Marketplace
http://www.fda.gov/news-events/press-announcements/new-fda-draft-guidance-aims-increase-safety-information-about-dietary-supplement-marketplace