Impella Generation 1 Purge Cassettes have an increased risk of purge leaks. Purge leaks can lead to low pump pressure and pump stops.
Impella Generation 1 Purge Cassettes have an increased risk of purge leaks. Purge leaks can lead to low pump pressure and pump stops.
The differential pressure sensor in certain Impella devices may malfunction and cause sensor values to drift.
FOR IMMEDIATE RELEASE – 03/30/2026 - Flushing, New York, Aphreseller (Ebay seller ID), Buy-herbal.com is recalling all lots of Kian Pee Wan capsules to the consumer level. FDA analysis has found that the product contains the undeclared drug ingredients dexamethasone and cyproheptadine. Products cont...
Navajo Manufacturing company is recalling certain heating pads that overheat when folded leading to potential burn injuries.
Erbe Cryoprobes may rupture during activation, leading to potential hearing loss, tinnitus, injury, or burns.
Bridgewater, New Jersey, Amneal Pharmaceuticals LLC is voluntarily recalling one lot of Magnesium Sulfate in Water for Injection, USP, 4g/100mL, IV bag, to the hospital level. A Magnesium Sulfate in Water for Injection pouch was found to contain an IV bag of Tranexamic Acid in 0.7% Sodium Chloride I...
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.
Certain SureForm Surgical Stapler reloads may form incomplete staple lines, leading to severe bleeding or death...
Omnipod Pods may not deliver insulin as intended due to a tear in the internal tubing...
Integra LifeSciences is removing certain lots of Microsensor and Cerelink ICP Kits with potential corrosion stains on the included Tuohy Needle.
Prismaflex Set deaeration chambers may dislodge from the Prismaflex Control Unit during use.
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...
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...
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...