Merit Medical Removes 16F Dual-Valved Splittable Sheath Introducer
This recall involves removing certain devices from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause serious injury or death if you continue to use it. Affected Product The FDA is aware that Merit Medical...Liquid Blenz Corp. Recalls Product Due to Possible Health Risk
Summary Company Announcement Date: April 06, 2026 FDA Publish Date: April 14, 2026 Product Type: Food & Beverages Carbonated Soft Drinks Foodborne Illness Reason for Announcement: Recall Reason Description Potential Foodborne Illness -Botulism Company Name:...FDA Issues Draft Guidance on Genome Editing Safety Standards to Advance Gene Therapy Development
For Immediate Release: April 14, 2026 The U.S. Food and Drug Administration today issued a draft guidance for sponsors seeking approval of human gene therapy products involving genome editing technologies. When finalized, this guidance will provide recommendations for...Rxgoodusa – 723622 – 04/01/2026
Recipient: Rxgoodusa United States Issuing Office: Center for Drug Evaluation and Research (CDER) United States WARNING LETTERApril 1, 2026MARCS-CMS 723622Rxgoodusa:This is to advise you that the United States (U.S.) Food and Drug Administration (FDA) recently...All Drug Purchases Are
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