SAN DIEGO – MAY 26, 2026 – DexCom, Inc. (Nasdaq: DXCM), the global leader in glucose biosensing, announced today through ongoing quality and accounting reviews it recently identified certain lots of Dexcom G7 sensors originally designated as scrap and intended for destruction were stolen during the...
If the hand controls to adjust the bed are not locked, children could adjust the bed and become entrapped.
Erbe Cryoprobes may rupture during activation, leading to potential hearing loss, tinnitus, injury, or burns.
Philips Trilogy Evo Ventilators may not function as intended if used with certain nebulizers.
Black specks and particulate matter have been reported in the drip chamber of certain ICU Medical IV tubing sets...
Specific Impella CP Sets are out of specification; use may result in low purge pressure events from the onset of the case...
Arrow International is removing dialysis catheter kits containing recalled Merit Medical Splittable Sheath Introducers...
Particulates have the potential to be introduced into blood circulation and become lodged within blood vessels.
ACTON, Mass.--(BUSINESS WIRE)-- Insulet Corporation, Inc. (NASDAQ: PODD) (“Insulet” or the “Company”) today announced a voluntary Medical Device Correction for specific lots of Omnipod® 5, Omnipod DASH®, and Omnipod® Insulin Management System (Omnipod Eros) Pods due to a manufacturing issue, identif...
React Health is removing affected devices due to a manufacturing process deviation that may result in an undetected oxygen leak condition.
A software error may cause the Automated Impella Controller to restart when used in conjunction with left ventricular Impella devices.
Certain labels used with i.v.STATION automated compounding systems may not be detected, leading to mislabeled sterile filled syringes.
Affected grafts may not unclasp from the delivery system. This may require conversion to open surgical repair and can result in patient death.
FDA alerts of?risks with use TRUE METRIX Blood Glucose Monitoring Systems by Trividia Health.
Trividia recommends that device users who receive an E-5 error code and are experiencing symptoms of high glucose should seek medical care immediately.
Draeger is correcting additional anesthesia workstations due to a manufacturing error that may cause the ventilator to fail before or during use.
FOR IMMEDIATE RELEASE MUMBAI, INDIA and PRINCETON, NJ - May 13, 2026 – Sun Pharma is voluntarily recalling within the U.S. to the hospital/user level, one batch of DOXOrubicin Hydrochloride Liposome Injection 50mg/25 mL, Lot # HAG2581B, Expiration 05/2027 (675 vials). The single batch of 675 vials i...
- May/8/2026- Jackson, WI, Pharmacal is recalling one lot of MG217 Multi-symptom Treatment Cream & Skin Protectant Eczema Cream, 6oz tube to the consumer level. The product has been found to be contaminated with Staphylococcus aureus.
The adaptor on Namic RA syringes may unwind during use. The resulting loose connection or disconnection may lead to infection, blood loss, or air embolism.
The adaptor on Namic RA syringes may unwind during use. The resulting loose connection or disconnection may lead to infection, blood loss, or air embolism.