FDA Med Watch
FDA Med Watch
The feed below is an automatic RSS feed from the FDA website.
- Glucose Monitor Sensor Recall: Abott Diabetes Care Removes Certain FreeStyle Libre 3 and FreeStyle Libre 3 Plus Sensors
- Early Alert: Heart Pump Issue from Abiomed
- Early Alert: Wound and Burn Dressing Issue from Integra LifeSciences
- Early Alert: Insufflation Unit Issue from Olympus
- Early Alert: Broselow Rainbow Tape Issue from AirLife
- Anesthesia Kit Recall: Medline Removes Anesthesia Circuits and Anesthesia Circuit Kits
- Early Alert: Stent and Electrocautery-Enhanced Delivery System Issue from Boston Scientific
- Olympus Expands Voluntary Recall for ViziShot 2 FLEX (19G) EBUS -TBNA Needles
- Anesthetic Vaporizer Recall: Draeger Removes Vapor 2000 and Vapor 3000 Vaporizers
- Abbott Initiates Medical Device Correction for Certain FreeStyle Libre® 3 and FreeStyle Libre 3 Plus Sensors in the U.S.
- Early Alert: Dialysis Tubing Set Issue from Vantive
- Anthony Trinh, 123Herbals LLC (123HERBALS.COM) Issues Nationwide Recall of Silintan Capsules Due to the Presence of Undeclared Meloxicam
- Organ Recovery Pack Correction: AVID Medical Issues Correction for Medical Convenience and Organ Recovery Kits
- Modern Warrior Recalls “Modern Warrior Ready” Dietary Supplement Due to Undeclared 1,4-DMAA and Aniracetam, as Well as Tianeptine, Which has Not Been Approved for Supplement Use by the FDA.
- Intravascular PICC Catheter Recall: Bard Removes PowerPICC Intravascular Catheters