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Medical Devices Recalls

Medical equipment, implants, and diagnostic devices

38,779 Total Recalls

This voluntary recall is due to reported complaints (<0.0025% of all in scope distributed product) indicating that there is an increased incidence of specific lots of the 15 mm Sheridan connector becoming disconnected from the Endotracheal tube.

May 24, 2019 Other Medical Devices Nationwide View Details →

Multiple complaints were received for balloons bursting below the rated burst pressure. Potential adverse events that may occur if an affected product is used include a delay in the procedure, additional intervention, vessel injury, and balloon fragmentation in the patient.

May 24, 2019 Surgical Instruments Nationwide View Details →

Incorrect part description contained on an additional label placed on the packaging: A 14mm length part was incorrectly labeled as being a 12mm length screw

Apr 1, 2019 Surgical Instruments Nationwide View Details →

AUTION HYBRID AU-4050

Arkray Factory USA

Class I - Dangerous

This correction is being initiated due to a software issue which results in the possibility of incorrect patient information being assigned to sample results when the following rare combination of three specific events were to occur: 1) No measurement results are generated due to an error by a urine sediment measurement. 2) The instrument is shutdown incorrectly. 3) An item rack is used for subsequent sample measurements.

May 3, 2019 Other Medical Devices View Details →

This voluntary recall is due to reported complaints (<0.0025% of all in scope distributed product) indicating that there is an increased incidence of specific lots of the 15 mm Sheridan connector becoming disconnected from the Endotracheal tube.

May 24, 2019 Other Medical Devices Nationwide View Details →

Possible corrosion of the battery contact(s).

May 10, 2019 Diagnostic Equipment Nationwide View Details →

Possibility of balloon rupture in intra-aortic occlusion devices. If the balloon bursts during cardiopulmonary bypass, the heart can fill and warm, the operative site may be obscured, and the device will need to be exchanged or operative strategy would need to change, including placement of an external cross-clamp, conversion to an open procedure, or performing the procedure under fibrillation.

May 14, 2019 Other Medical Devices Nationwide View Details →

Weld attaching the air heater assembly to the main sterilizer unit has shown signs of fatigue/failure

Apr 18, 2019 Other Medical Devices Nationwide View Details →

Possibility that inlet pump hose of the Washer Disinfector Getinge 86-Series (S-8666, S-8668) might collapse during use result in low water pressure within the circulation system and, in the worst case scenario, can result in the contents of the Washer Disinfector not being cleaned properly after finished process.

May 20, 2019 Surgical Instruments Nationwide View Details →

There has been a reported incident of a Distar CRT monitor that has fallen off the monitor wall mount related to product aging.

Mar 29, 2019 Infusion Pumps Nationwide View Details →