FDA Device recall Z-0081-2021
Biomet Regenerex Primary Taper Cap Item Number 141269
- FDA Device
- Class II
- terminated
- Published 2020-10-14
On 2020-10-14 the FDA classified a Class II recall of Biomet Regenerex Primary Taper Cap Item Number 141269 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-0081-2021 |
| 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 Regenerex Primary Taper Cap Item Number 141269
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: 015800 324440 685300 023900 324440R 696280 058930 389060 821980 200720 418430 890320 313260 646040 997610 |
|---|
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-0081-2021%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.