Biomet, Inc.: Medical Device Recall in 2020 - (Recall #: Z-0081-2021)

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:

Biomet Regenerex Primary Taper Cap Item Number 141269

Product Classification:

Class II

Date Initiated: September 4, 2020

Date Posted: October 14, 2020

Recall Number: Z-0081-2021

Event ID: 86424

Reason for Recall:

Product not properly being aligned with the adequate gamma sterilization group and result in the product not being properly sterilized

Status: Terminated

Product Quantity: US: 62 units; OUS: 176 units

Code Information:

Lot Numbers: 015800 324440 685300 023900 324440R 696280 058930 389060 821980 200720 418430 890320 313260 646040 997610

Distribution Pattern:

Nationwide Foreign: Canada, FINLAND, NETHERLANDS, UNITED KINGDOM

Voluntary or Mandated:

Voluntary: Firm initiated