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Medical Devices Recalls

Medical equipment, implants, and diagnostic devices

38,779 Total Recalls

The instruments are not able to pass instrument verification which is performed prior to the use of each instrument.

Jun 29, 2017 Diagnostic Equipment Nationwide View Details →

Medtronic received reports that the DBS depth stop did not adequately secure to the lead, which can result in DBS lead placement beyond the intended target.

Mar 17, 2017 Implants & Prosthetics Nationwide View Details →

The instruments are not able to pass instrument verification which is performed prior to the use of each instrument.

Jun 29, 2017 Diagnostic Equipment Nationwide View Details →

The firm manufactured and distributed custom surgical kits which contained BD SafetyGlide" 22GA 1Âŋ inch Needles. BD subsequently recalled these needles because, " Loose polypropylene particulate in the fluid path could be expelled out of the needle during injection.

Jun 15, 2017 Surgical Instruments Nationwide View Details →

Error in reprocessing instructions in Revisions 13 and 14 of IFU Z845, used with EG-3670URK and EG-3870UTK ultrasound gastroscopes. In the disinfection step, the IFU has a warning indicating the cleaning detergent solution should remain in contact with the all internal channels and external endoscope surfaces. The disinfecting solution, not the cleaning detergent, should be used for this step.

May 23, 2017 Diagnostic Equipment Nationwide View Details →

The instruments are not able to pass instrument verification which is performed prior to the use of each instrument.

Jun 29, 2017 Diagnostic Equipment Nationwide View Details →

Potential inaccurate calibration by service depot repair, which could contribute to patients being burnt by the device. This only impacts units serviced between the dates of 09/08/2016 and 05/23/2017.

Jun 1, 2017 Other Medical Devices View Details →

The instruments are not able to pass instrument verification which is performed prior to the use of each instrument.

Jun 29, 2017 Diagnostic Equipment Nationwide View Details →

The instruments are not able to pass instrument verification which is performed prior to the use of each instrument.

Jun 29, 2017 Diagnostic Equipment Nationwide View Details →

Potential inaccurate calibration by service depot repair, which could contribute to patients being burnt by the device. This only impacts units serviced between the dates of 09/08/2016 and 05/23/2017.

Jun 1, 2017 Other Medical Devices View Details →

The instruments are not able to pass instrument verification which is performed prior to the use of each instrument.

Jun 29, 2017 Diagnostic Equipment Nationwide View Details →

The instruments are not able to pass instrument verification which is performed prior to the use of each instrument.

Jun 29, 2017 Diagnostic Equipment Nationwide View Details →

Error in reprocessing instructions in Revisions 13 and 14 of IFU Z845, used with EG-3670URK and EG-3870UTK ultrasound gastroscopes. In the disinfection step, the IFU has a warning indicating the cleaning detergent solution should remain in contact with the all internal channels and external endoscope surfaces. The disinfecting solution, not the cleaning detergent, should be used for this step.

May 23, 2017 Diagnostic Equipment Nationwide View Details →