FDA-Device2020-10-14Class II

Biomet ARTHROSIMPLICITY KIT EU Item Number: 24-4055

Biomet, Inc.
Hazard

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

Sold states
Nationwide Foreign: Canada, FINLAND, NETHERLANDS, UNITED KINGDOM
Affected count
4 units OUS
Manufactured in
56 E Bell Dr, N/A, Warsaw, IN, United States
Products
Biomet ARTHROSIMPLICITY KIT EU Item Number: 24-4055

Official notice

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0084-2021

Don't want to check this manually?

We email you a Sunday digest of new federal recalls relevant to parents — free, no credit card. Or upgrade to as-it-happens alerts for the brands you actually own.

Get the Sunday Brief