DUBLIN, Ohio, March 19, 2026 – Cardinal Health has issued a voluntary recall for select lots of Webcol™ Large Alcohol Prep Pads (70% isopropyl alcohol) to the consumer level. The product is being recalled due to microbial contamination identified as Paenibacillus phoenicis.

Navajo Manufacturing company is recalling certain heating pads that overheat when folded leading to potential burn injuries

Omnipod Pods may not deliver insulin as intended due to a tear in the internal tubing

Certain SureForm Surgical Stapler reloads may form incomplete staple lines, leading to severe bleeding or death

Prismaflex Set deaeration chambers may dislodge from the Prismaflex Control Unit during use.

Integra LifeSciences is removing certain lots of Microsensor and Cerelink ICP Kits with potential corrosion stains on the included Tuohy Needle.

ACTON, Mass.--(BUSINESS WIRE)-- Insulet Corporation (NASDAQ: PODD) (“Insulet” or the “Company”) today initiated a voluntary Medical Device Correction for specific lots of Omnipod® 5 Pods after identifying a manufacturing issue through its ongoing product monitoring. This action applies to specific i

Erbe Cryoprobes may rupture during activation, leading to potential hearing loss, tinnitus, injury, or burns

Integra is removing certain Wound and Burn Dressing products that may have breached sterile barriers.

Certain reprocessed catheters may contain residual particulates that could cause infection, embolism, or thrombosis.

Certain reprocessed catheters may contain residual particulates that could cause infection, embolism, or thrombosis

These choking rescue protocols include abdominal thrusts (also called the “Heimlich” maneuver) for children and adults but not anti-choking devices.

Boston Scientific is removing certain stents and delivery systems due to issues with deployment and expansion.

Fresenius Kabi is correcting Ivenix LVP software due to anomalies that could cause serious patient harm or death

Impella Generation 1 Purge Cassettes have an increased risk of purge leaks. Purge leaks can lead to low pump pressure and pump stops

Olympus is removing certain High Flow Insufflation Unit models due to software issues that may lead to overpressure events.

Trividia recommends that device users who receive an E-5 error code and are experiencing symptoms of high glucose should seek medical care immediately  

Medline updates use instructions for Electronic Homecare Beds due to risk of electrical fires and entrapment.

AirLife is removing Broselow Rainbow Tapes due to incorrectly printed medication dosing information.

FT. LAUDERDALE, FL) – February 6, 2026 – Trividia Health, Inc., announced today that it is initiating a labeling correction which requires a modification of the Owner’s Booklets/System Instructions for Use for all TRUE METRIX, TRUE METRIX AIR, TRUE METRIX GO, and TRUE METRIX PRO Blood Glucose Monit