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Medical Devices Recalls

Medical equipment, implants, and diagnostic devices

38,779 Total Recalls

Beckman coulter has received complaints regarding leaking and cracked C cups. When the cup cracks, coolant can leak onto the connectors of the Printed Circuit Boards (PCB) in the analyzer, resulting in a short-circuit causing the instrument to go into a stop mode.

Jul 30, 2015 Other Medical Devices Nationwide View Details →

The manufacturing and expiration dates are not printed on the blister pack label.

Aug 8, 2013 Implants & Prosthetics View Details →

Branan Medical is recalling the AmediCheck Instant Test Cup, a 5 panel drug cup, because it may erroneously contain 12 panel cups due to a packaging error.

Jul 5, 2016 Diagnostic Equipment Nationwide View Details →

The surface coating applied to the device is blistering, peeling and discoloring after usage over time

Jul 4, 2016 Implants & Prosthetics Nationwide View Details →

Medtronic Navigation, Inc. announces a voluntary field action for the Medtronic Navigation StealthStation Software applications affected by Neurologica BodyTom/CereTom floor-based scanners.

Jul 18, 2016 Implants & Prosthetics Nationwide View Details →

A total of 70 6F/7F Mynx Grip devices were shipped from a distributor using improper transport/packaging configurations.

Jul 13, 2016 Diagnostic Equipment View Details →

The firm has received multiple reports of the Non-Invasive Blood Pressure (NIBP) parameter becoming non-functional with an associated message (No Reading). In addition, there is one of the following three error messages: Inflate Error, HW Error, or No Data.

Jul 1, 2016 Patient Monitors View Details →

Trigger lock option does not always prevent x-ray generation. Specifically if the unit is in test mode or repeat test mode then the trigger lock may not prevent x-ray initiation when the trigger is pulled. The correction is via repair by a software update.

Jun 22, 2016 Other Medical Devices Nationwide View Details →

Medtronic Navigation, Inc. announces a voluntary field action for the Medtronic Navigation StealthStation Software applications affected by Neurologica BodyTom/CereTom floor-based scanners.

Jul 18, 2016 Implants & Prosthetics Nationwide View Details →

Roche Diagnostics Operations, Inc. has issued a voluntary recall for the Online TDM Vancomycin assay on the cobas c 311/501/502 analyzers and the Modular Analytics P module due method sheets that state an incorrect method comparison against the COBAS INTEGRA 800 analyzer.

May 26, 2016 Diagnostic Equipment Nationwide View Details →

Medtronic Navigation, Inc. announces a voluntary field action for the Medtronic Navigation StealthStation Software applications affected by Neurologica BodyTom/CereTom floor-based scanners.

Jul 18, 2016 Implants & Prosthetics Nationwide View Details →

The surface coating applied to the device is blistering, peeling and discoloring after usage over time

Jul 4, 2016 Implants & Prosthetics Nationwide View Details →

Merge HEMO software.

Merge Healthcare

Class I - Dangerous

The International Normalized Ratio (INR) value displayed in the study report does not match the value that is imported on the pre-procedure labs screen from HL7

Jul 2, 2012 Other Medical Devices Nationwide View Details →

The surface coating applied to the device is blistering, peeling and discoloring after usage over time

Jul 4, 2016 Implants & Prosthetics Nationwide View Details →

The surface coating applied to the device is blistering, peeling and discoloring after usage over time

Jul 4, 2016 Implants & Prosthetics Nationwide View Details →

If an affected Patient Monitor has been powered on continuously for several months, any displayed waveforms will contain outdated data and therefore fail to reflect the patients current condition.

Jul 26, 2016 Diagnostic Equipment Nationwide View Details →