Zimmer Biomet, Inc.: Medical Device Recall in 2019 - (Recall #: Z-0298-2020)

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:

BF Humeral Stem, Various Sizes, Item Nos. 00430000606 00430000613 00430000706 00430000713 00430000813 00430000817 00430000820 00430000913 00430001013 00430001017 00430001020 00430001113 00430001213 00430001217 00430001220 00430001313 00430001413 00430001417 00430001420 00430001513 00430001613 00430001713 00430001813 47430103100

Product Classification:

Class II

Date Initiated: October 10, 2019

Date Posted: November 13, 2019

Recall Number: Z-0298-2020

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