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.
When the sizing catheters are used during angiographic procedures the marker bands may be at an increased risk of cracking/breakage.
When?the?Volara?system is used?in a home setting, there is a risk for oxygen desaturation or barotrauma?if it is used in-line with a ventilator.
Santa Fe Springs, California – April 07, 2026 – Blaine Labs, Inc. is voluntarily recalling three (3) lot numbers of Wound Care Gel products, 1 oz. & 3 oz. (0.1% Benzalkonium Chloride) to the consumer level due to microbial contamination.
The differential pressure sensor in certain Impella devices may malfunction and cause sensor values to drift.
Impella Generation 1 Purge Cassettes have an increased risk of purge leaks. Purge leaks can lead to low pump pressure and pump stops.
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.
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...
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.