Zimmer Biomet, Inc.: Medical Device Recall in 2016 - (Recall #: Z-0317-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Zimmer¿ Gender Solutions" Patellofemoral Joint Prosthesis Milling Handpiece

Product Classification:

Class II

Date Initiated: September 28, 2016

Date Posted: November 2, 2016

Recall Number: Z-0317-2017

Event ID: 75371

Reason for Recall:

Complaints have been reported that the handpiece is inoperable. The investigation found that the complaints were related to the lack of preventative maintenance contrary to what is recommended in the instructions for use included with the handpiece. An inoperable device may lead to a delay in surgery

Status: Terminated

Product Quantity: 703

Code Information:

Item Number 00-5927-040-00 Serial Number All

Distribution Pattern:

Nationwide. CANADA HONG KONG KOREA SINGAPORE CHINA VENEZUELA AUSTRALIA JAPAN NETHERLANDS GERMANY INDIA TAIWAN

Voluntary or Mandated:

Voluntary: Firm initiated