Zimmer Biomet, Inc.: Medical Device Recall in 2018 - (Recall #: Z-0803-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

The 2nd Assist Knee Positioner

Product Classification:

Class II

Date Initiated: September 7, 2017

Date Posted: March 7, 2018

Recall Number: Z-0803-2018

Event ID: 79141

Reason for Recall:

Zimmer Biomet is conducting a medical device recall for the 2nd Assistant Knee Positioner due to the potential for the sterile packaging barrier to be breached during distribution.

Status: Terminated

Product Quantity: 38,879 units

Code Information:

Item# 740026

Distribution Pattern:

Nationally

Voluntary or Mandated:

Voluntary: Firm initiated