Zimmer, Inc.: Medical Device Recall in 2014 - (Recall #: Z-0784-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

Zimmer Segmental Systems; Polyethylene Inserts, Size C. Knee replacement.

Product Classification:

Class II

Date Initiated: December 19, 2013

Date Posted: January 29, 2014

Recall Number: Z-0784-2014

Event ID: 66846

Reason for Recall:

After evaluation of 13 complaints(0.4% rate) for hyper-extension of the Zimmer Segmental System, Zimmer is updating the related surgical technique and instructions for use to provide additional instructions and patient conditions that may place excessive loading on the polyethylene insert.

Status: Terminated

Product Quantity: 5305 distribution events

Code Information:

Part numbers 00-5850-013-95

Distribution Pattern:

Worldwide Distribution. USA nationwide and Germany, with further distribution into EU countries.

Voluntary or Mandated:

Voluntary: Firm initiated