Swissmedic Batch Recall of Risperidon-Mepha LA Injection
What Changed? As of January 22, 2026, Swissmedic announced a batch recall of Risperidon-Mepha LA Pulver und Lösungsmittel zur Herstellung […]
FDA Issues Early Alert for Broselow Rainbow Tape Due to Medication Errors
The FDA has issued an early alert regarding a potentially high-risk device issue with the Broselow Rainbow Tape, a color-coded
FDA Issues Urgent Recall of Draeger Vapor 2000 and Vapor 3000 Anesthetic Vaporizers
The US Food and Drug Administration (FDA) has announced an urgent recall of certain Draeger Vapor 2000 and Vapor 3000
Olympus Expands Voluntary Recall of ViziShot 2 FLEX EBUS-TBNA Needles Due to Device Component Ejection
OLYMPUS CORPORATION has expanded its voluntary recall of the ViziShot 2 FLEX (19G) EBUS-TBNA needles due to reports of device
FDA Issues Urgent Recall of Medline Anesthesia Kits Due to Potential for Serious Injury or Death
On January 17, 2026, the FDA announced an urgent recall of certain Medline anesthesia kits due to the potential for
FDA Issues Early Alert for Boston Scientific’s Stent and Electrocautery-Enhanced Delivery System
As of January 22, 2026, the FDA has issued an early alert regarding a potentially high-risk device issue with Boston
FDA Issues Early Alert for Olympus Insufflation Units Due to Potential Overpressure Risks
An important medical device safety announcement was made on January 26, 2026, regarding certain Olympus insufflation units. Healthcare professionals and
FDA Issues Early Alert for Integra LifeSciences’ Wound and Burn Dressing Products
As of January 23, 2026, the FDA has issued an early alert regarding a potentially high-risk device issue with Integra
FDA Initiates Steps to Enhance Gluten Disclosure in Food Products
Meta description: FDA improves gluten ingredient disclosure in foods. Published on 2026-01-26. The US Food and Drug Administration has issued