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Medical Devices Recalls

Medical equipment, implants, and diagnostic devices

38,779 Total Recalls
Class I - Dangerous

During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.

Aug 7, 2017 Implants & Prosthetics Nationwide View Details β†’

During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.

Aug 7, 2017 Implants & Prosthetics Nationwide View Details β†’

During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.

Aug 7, 2017 Implants & Prosthetics Nationwide View Details β†’
Class I - Dangerous

During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.

Aug 7, 2017 Implants & Prosthetics Nationwide View Details β†’

During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.

Aug 7, 2017 Implants & Prosthetics Nationwide View Details β†’
Class I - Dangerous

During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.

Aug 7, 2017 Implants & Prosthetics Nationwide View Details β†’

During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.

Aug 7, 2017 Implants & Prosthetics Nationwide View Details β†’

During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.

Aug 7, 2017 Implants & Prosthetics Nationwide View Details β†’

During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.

Aug 7, 2017 Implants & Prosthetics Nationwide View Details β†’
Class I - Dangerous

During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.

Aug 7, 2017 Implants & Prosthetics Nationwide View Details β†’
Class I - Dangerous

During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.

Aug 7, 2017 Implants & Prosthetics Nationwide View Details β†’

CARESCAPE Central Station (CSCS) software version 2.0.2 units may experience unexpected NO COMM (No Communication) and network communication issues after boot-up or system restart.

Jan 11, 2018 Diagnostic Equipment Nationwide View Details β†’

This recall has been initiated due to a potential malfunction of the photo interrupter (Pl). The potential malfunction has been attributed to aging and premature deterioration of the Pl collector current.

Jun 11, 2017 Diagnostic Equipment Nationwide View Details β†’

During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.

Aug 7, 2017 Implants & Prosthetics Nationwide View Details β†’
Class I - Dangerous

During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.

Aug 7, 2017 Implants & Prosthetics Nationwide View Details β†’
Class I - Dangerous

During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.

Aug 7, 2017 Implants & Prosthetics Nationwide View Details β†’

During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.

Aug 7, 2017 Implants & Prosthetics Nationwide View Details β†’