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Implants & Prosthetics

πŸ₯ Medical Devices β€’ 4,540 recalls

Stryker received a report from the field indicating that a citation TMZF HA 132 degrees neck angle V40 Hip Stem - Left Size # 4 was identified in a packaging associated with a citation TMZF HA 132 degrees Neck Angle V40 Hip Stem - Right Size #3.

Feb 3, 2014 Implants & Prosthetics Nationwide View Details β†’

Discovery of serious injuries and deaths associated with the process of changing from a primary System controller to their back-up System controller in patients using the Pocket System controller model.

Mar 4, 2014 Implants & Prosthetics Nationwide View Details β†’

The products are being recalled because they did not meet minimum needle attachment strength requirements.

Mar 11, 2014 Implants & Prosthetics Nationwide View Details β†’

Discovery of serious injuries and deaths associated with the process of changing from a primary System controller to their back-up System controller in patients using the Pocket System controller model.

Mar 4, 2014 Implants & Prosthetics Nationwide View Details β†’

Communication to European physician users of the Ovation Prime Abdominal Stent Graft system to notify them of changes to Instructions for Use.

Feb 27, 2014 Implants & Prosthetics View Details β†’

A complaint was received for a discolored All Poly Tibia. Root cause analysis found that the discoloration was the result of free radical oxidation. The oxidation process was advanced prematurely as a result of the machined component being stored in a transparent container exposed to artificial light for six years prior to inert packaging and sterilization of the device.

Feb 25, 2014 Implants & Prosthetics Nationwide View Details β†’

Reports relating to Biomet 3i's BellaTek Zirconia Dental Abutment fractures were received.

Aug 26, 2013 Implants & Prosthetics Nationwide View Details β†’

A complaint was received for a discolored All Poly Tibia. Root cause analysis found that the discoloration was the result of free radical oxidation. The oxidation process was advanced prematurely as a result of the machined component being stored in a transparent container exposed to artificial light for six years prior to inert packaging and sterilization of the device.

Feb 25, 2014 Implants & Prosthetics Nationwide View Details β†’

The firm was notified by a customer of a cracked spring in the handle of the RCD1 device.

Jan 23, 2014 Implants & Prosthetics Nationwide View Details β†’

A complaint was received for a discolored All Poly Tibia. Root cause analysis found that the discoloration was the result of free radical oxidation. The oxidation process was advanced prematurely as a result of the machined component being stored in a transparent container exposed to artificial light for six years prior to inert packaging and sterilization of the device.

Feb 25, 2014 Implants & Prosthetics Nationwide View Details β†’

A complaint was received for a discolored All Poly Tibia. Root cause analysis found that the discoloration was the result of free radical oxidation. The oxidation process was advanced prematurely as a result of the machined component being stored in a transparent container exposed to artificial light for six years prior to inert packaging and sterilization of the device.

Feb 25, 2014 Implants & Prosthetics Nationwide View Details β†’

A complaint was received for a discolored All Poly Tibia. Root cause analysis found that the discoloration was the result of free radical oxidation. The oxidation process was advanced prematurely as a result of the machined component being stored in a transparent container exposed to artificial light for six years prior to inert packaging and sterilization of the device.

Feb 25, 2014 Implants & Prosthetics Nationwide View Details β†’

A complaint was received for a discolored All Poly Tibia. Root cause analysis found that the discoloration was the result of free radical oxidation. The oxidation process was advanced prematurely as a result of the machined component being stored in a transparent container exposed to artificial light for six years prior to inert packaging and sterilization of the device.

Feb 25, 2014 Implants & Prosthetics Nationwide View Details β†’