FDA Device recall Z-0084-2021
Biomet ARTHROSIMPLICITY KIT EU Item Number: 24-4055
- FDA Device
- Class II
- terminated
- Published 2020-10-14
On 2020-10-14 the FDA classified a Class II recall of Biomet ARTHROSIMPLICITY KIT EU Item Number: 24-4055 by Biomet, citing product not properly being aligned with the adequate gamma sterilization group and result in the product not being properly sterilized.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0084-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-09-04 |
| Published | 2020-10-14 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Biomet |
| Distribution | US |
Product
Biomet ARTHROSIMPLICITY KIT EU Item Number: 24-4055
Reason
Product not properly being aligned with the adequate gamma sterilization group and result in the product not being properly sterilized
Identifiers
| code_info | Lot Numbers: 894660A 894660B 894670B 894700B |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0084-2021%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.