Zimmer Biomet, Inc.: Medical Device Recall in 2019 - (Recall #: Z-0314-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Periarticulare Plates - Elbow, Humeral and Ulna Plates, Item Nos. 00234800504 00234800506 00234800508 00234800510 00234800512 00234800514 00234800604 00234800606 00234800608 00234800610 00234800612 00234800614 00234800712 00234800714 00234800716 00234800902 00234800904 00234800906 00234800908 00234800910 00234800912 00234800914 00234801002 00234801004 00234801006 00234801008 00234801010 00234801012

Product Classification:

Class II

Date Initiated: October 10, 2019

Date Posted: November 13, 2019

Recall Number: Z-0314-2020

Event ID: 83962

Reason for Recall:

Non-highly polished implants may adhere to the LDPE bag (previous packaging configuration).

Status: Terminated

Product Quantity: 5,459,583 total devices

Code Information:

All product manufactured prior to January 2014.

Distribution Pattern:

Distributed nationwide.

Voluntary or Mandated:

Voluntary: Firm initiated