Zimmer Biomet, Inc.: Medical Device Recall in 2019 - (Recall #: Z-0313-2020)

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:

PERIARTICULAR PLATES SHOULDER, PERI PROX LAT HUMERAL, Item Nos. 00234800104 00234800106 00234800108 00234800110 00234800112 00234800114 00234800116 00234800204 00234800206 00234800208 00234800210 00234800212 00234800214 00234800216 00234800304 00234800306 00234800404 00234800408 00234800412

Product Classification:

Class II

Date Initiated: October 10, 2019

Date Posted: November 13, 2019

Recall Number: Z-0313-2020

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