FDA Device recall Z-2242-2021
smith&nephew BHR SQUARE HEADED NAIL, REF CATALOG NUMBER 999908
- FDA Device
- Class II
- terminated
- Published 2021-08-18
On 2021-08-18 the FDA classified a Class II recall of smith&nephew BHR SQUARE HEADED NAIL, REF CATALOG NUMBER 999908 by Smith And Nephew Orthopaedics Aurora, citing the nail head may become detached during surgery.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2242-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-07-14 |
| Published | 2021-08-18 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Smith And Nephew Orthopaedics Aurora |
| Distribution | US |
Product
smith&nephew BHR SQUARE HEADED NAIL, REF CATALOG NUMBER 999908. For use during orthopedic surgery.
Reason
The nail head may become detached during surgery.
Identifiers
| code_info | Lot/Batch Codes: 20LW15962, 20LW15963 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2242-2021%22
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