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Medical Devices Recalls

Medical equipment, implants, and diagnostic devices

38,779 Total Recalls

The product packaging seal has the potential to experience seal creep. This may result in gaps to be created in the seals of the packaging and may impact the sterility of the Needle Counters.

Apr 24, 2018 Surgical Instruments Nationwide View Details →

Possible out of specification condition which may allow a bead component to separate from an adjacent wire link. This condition may result in a discontinuous or open LINX device.

Apr 20, 2018 Implants & Prosthetics Nationwide View Details →

An error was discovered in the interpretation of certain DICOM header tags that may lead to incorrect orientation labeling, and thus and indirect left-right, up-down or anterior-posterior flipping of images.

Dec 15, 2014 Diagnostic Equipment Nationwide View Details →

Lot J1 of the Syva¿ EMIT¿ 2000 Theophylline Assay, when run on a Beckman AU Clinical Chemistry System, may exhibit increased imprecision for commercially available controls and for patient samples.

Nov 27, 2017 Infusion Pumps Nationwide View Details →

Possible transient electrical connection interruption between an HVAD System power source (Battery, AC Adapter, or DC Adapter) and the Controller, while the power source is connected, that may cause unintended switching to the secondary power source and/or unexpected audible tones (beeping). The interruption typically lasts 1-2 seconds, due to oxidation between power source connector and socket.

May 2, 2018 Other Medical Devices Nationwide View Details →

There is a potential for the cord to spark and cause a fire.

Apr 17, 2018 Surgical Instruments Nationwide View Details →