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Medical Devices Recalls

Medical equipment, implants, and diagnostic devices

38,779 Total Recalls

PICC catheters that contain valve(s) manufactured prior to July 15, 2014 lack a manufacturing specification change that reduces the incidence of hemolysis during blood sampling through the PICC catheter.

Mar 14, 2016 Diagnostic Equipment Nationwide View Details →

CareFusion has identified a potential risk associated with AVEA Ventilator caused by an incorrect F1 fuse on the AVEA Ventilator Transducer Communication Alarm (TCA) Board which may fail/blow, causing loss of power to the User Interface Module (UIM).

May 17, 2016 Patient Monitors Nationwide View Details →

PICC catheters that contain valve(s) manufactured prior to July 15, 2014 lack a manufacturing specification change that reduces the incidence of hemolysis during blood sampling through the PICC catheter.

Mar 14, 2016 Infusion Pumps Nationwide View Details →

Zimmer Biomet is initiating a recall of specific lots of foil pouched, sterile Trabecular Metal implants that were manufactured between April 2011 and October 2012. The foil pouches are part of a dual barrier system to provide sterile integrity.

Apr 15, 2016 Other Medical Devices Nationwide View Details →

PICC catheters that contain valve(s) manufactured prior to July 15, 2014 lack a manufacturing specification change that reduces the incidence of hemolysis during blood sampling through the PICC catheter.

Mar 14, 2016 Infusion Pumps Nationwide View Details →

In some cases it has been difficult or not possible to disassemble the adjusted Dome Centric from the AS Humeral Rasp after initial positioning of the AS Humeral Trial Head which resulted in the whole construct of the Dome Centric with the still assembled AS Humeral Rasp taken out of the humeral canal. This could cause a delay in surgery time or the surgeon could decide to close the wound without finishing the surgery, increasing the infection risk or second use of anesthesia necessary.

May 17, 2016 Implants & Prosthetics Nationwide View Details →

PICC catheters that contain valve(s) manufactured prior to July 15, 2014 lack a manufacturing specification change that reduces the incidence of hemolysis during blood sampling through the PICC catheter.

Mar 14, 2016 Diagnostic Equipment Nationwide View Details →

Due to the lack of updated thermal components, these instruments may be more susceptible to the internal case temperature exceeding the 18 to 36 degrees Celsius operating range, causing SYS flags. The instrument will not report results until the internal case temperature returns to the operating range. This situation may cause a delay in the reporting of patient results.

May 17, 2016 Diagnostic Equipment View Details →

The bracket that is used to lift the cover has bolts that were not welded in potentially causing the cover to fall down during service.

Apr 25, 2016 Diagnostic Equipment Nationwide View Details →

The bracket that is used to lift the cover has bolts that were not welded in potentially causing the cover to fall down during service.

Apr 25, 2016 Diagnostic Equipment Nationwide View Details →

PICC catheters that contain valve(s) manufactured prior to July 15, 2014 lack a manufacturing specification change that reduces the incidence of hemolysis during blood sampling through the PICC catheter.

Mar 14, 2016 Diagnostic Equipment Nationwide View Details →

PICC catheters that contain valve(s) manufactured prior to July 15, 2014 lack a manufacturing specification change that reduces the incidence of hemolysis during blood sampling through the PICC catheter.

Mar 14, 2016 Diagnostic Equipment Nationwide View Details →

PICC catheters that contain valve(s) manufactured prior to July 15, 2014 lack a manufacturing specification change that reduces the incidence of hemolysis during blood sampling through the PICC catheter.

Mar 14, 2016 Diagnostic Equipment Nationwide View Details →

PICC catheters that contain valve(s) manufactured prior to July 15, 2014 lack a manufacturing specification change that reduces the incidence of hemolysis during blood sampling through the PICC catheter.

Mar 14, 2016 Diagnostic Equipment Nationwide View Details →

Zimmer Biomet is initiating a recall of specific lots of foil pouched, sterile Trabecular Metal implants that were manufactured between April 2011 and October 2012. The foil pouches are part of a dual barrier system to provide sterile integrity.

Apr 15, 2016 Other Medical Devices Nationwide View Details →

CareFusion has identified a potential risk associated with AVEA Ventilator caused by an incorrect F1 fuse on the AVEA Ventilator Transducer Communication Alarm (TCA) Board which may fail/blow, causing loss of power to the User Interface Module (UIM).

May 17, 2016 Patient Monitors Nationwide View Details →