Zimmer Biomet, Inc.: Medical Device Recall in 2019 - (Recall #: Z-0308-2020)

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 - FEMUR, Item Nos. 00234700106 00234700108 00234700110 00234700112 00234700114 00234700116 00234700118 00234700206 00234700208 00234700210 00234700212 00234700214 00234700216 00234700218 00234703104 00234703106 00234703108 00234703204 00234703206 00234703208

Product Classification:

Class II

Date Initiated: October 10, 2019

Date Posted: November 13, 2019

Recall Number: Z-0308-2020

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