Zimmer Biomet, Inc.: Medical Device Recall in 2020 - (Recall #: Z-0057-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Dual Mobility Vivacit-E Bearing, Model Number 110031009

Product Classification:

Class II

Date Initiated: August 14, 2020

Date Posted: October 14, 2020

Recall Number: Z-0057-2021

Event ID: 86404

Reason for Recall:

The outer package is labeled as a Size C 38 mm, however, the implant inside the package is a Size E 42 mm.

Status: Terminated

Product Quantity: 31

Code Information:

Lot Number 64755636

Distribution Pattern:

Products were distributed to the following US states: FL, ID, IL, IN, KY, MA, MD, MI, MN, NC, NJ, OH, OR, PA, SC, TX, UT, VA, WI, and WV.

Voluntary or Mandated:

Voluntary: Firm initiated