FDA Device recall Z-0083-2021
Biomet ONPOINT SCOPE PROCEDURE KIT-EU Item Number: 24-3055
- FDA Device
- Class II
- terminated
- Published 2020-10-14
On 2020-10-14 the FDA classified a Class II recall of Biomet ONPOINT SCOPE PROCEDURE KIT-EU Item Number: 24-3055 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-0083-2021 |
| 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 ONPOINT SCOPE PROCEDURE KIT-EU Item Number: 24-3055
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: 866270A 887060B 919100B 938510A 942310A 905460A 907080A 930110A 866270B 887070A 919110A 938510…Lot Numbers: 866270A 887060B 919100B 938510A 942310A 905460A 907080A 930110A 866270B 887070A 919110A 938510B 942310B 905460B 907080B 930110B 866280A 887070B 919110B 938520A 942320A 905470A 907090A 930120A 866280B 887080A 919120A 938520B 942320B 905470B 907090B 930120B 866290A 887080B 919120B 938530A 942330A 905480A 907100A 930130A 866290B 887090A 919130A 938530B 942330B 905480B 907100B 930130B 866300A 887090B 919130B 938540A 942340B 905490A 907110A 930140A 866300B 887100A 920410A 938540B 946900A 905490B 907110B 930140B 866310A 887100B 920410B 942150A 946900B 905500A 907120A 934570A 866310B 902920A 920420A 942150B 946910A 905500B 907120B 934570B 866320A 902920B 920420B 942160A 946910B 905520A 907130A 934580A 866320B 902930A 920430A 942160B 946930B 905520B 926660A 934580B 866330A 907130B 920430B 942180A 946940A 905530A 926660B 934590A 866330B 915230A 920440A 942180B 946950B 90553 |
|---|
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-0083-2021%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.