Biomet, Inc.: Medical Device Recall in 2020 - (Recall #: Z-0084-2021)

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 ARTHROSIMPLICITY KIT EU Item Number: 24-4055

Product Classification:

Class II

Date Initiated: September 4, 2020

Date Posted: October 14, 2020

Recall Number: Z-0084-2021

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: 4 units OUS

Code Information:

Lot Numbers: 894660A 894660B 894670B 894700B

Distribution Pattern:

Nationwide Foreign: Canada, FINLAND, NETHERLANDS, UNITED KINGDOM

Voluntary or Mandated:

Voluntary: Firm initiated