All Recalls

95,089 total recalls in our database

Vascular Solutions is recalling Twin-Pass dual access catheters because there is a potential for excess manufacturing material to remain at the tip of the catheter or within the distal portion of the rapid exchange lumen.

Sep 16, 2016 Diagnostic Equipment Nationwide View Details β†’

The Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES, Part # 13140, of the custom AMS kit were recalled because gloves may contain splits or holes compromising sterility.

Apr 22, 2015 Other Medical Devices Nationwide View Details β†’
πŸ₯ Medical Devices Class I - Dangerous

New warning requiring Users to conduct duodenoscope precleaning and manual cleaning even when using an Automated Endoscope Reprocessor (AER) that has instructions that may indicate a user could forego certain steps in precleaning and manual cleaning of the endoscopes.

Jun 23, 2016 Other Medical Devices Nationwide View Details β†’

A number of Agee WristJackΒΏ Fracture Reduction Systems have been manufactured with a molded beam slightly larger than optimal. This may result in the surgeon experiencing difficulty fine-tuning the length (red) and radial/ulnar alignment (blue) adjustments on the device.

Sep 14, 2016 Implants & Prosthetics Nationwide View Details β†’