PERI-LOC VOLAR DISTAL RADIUS — Class II medical device recall Z-2036-2017
Terminated recall by Smith & Nephew, Inc., reported 2017-05-17. This lot of left plates were laser etched and packaged as right plates.
| Recall number | Z-2036-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Smith & Nephew, Inc., Memphis, TN, United States |
| Recall initiated | 2017-03-22 |
| Classified | 2017-05-05 |
| Reported by FDA | 2017-05-17 |
| Terminated | 2022-06-03 |
| Countries outside the US | IN |
| Quantity | 12 units |
| Lot numbers | 16DM15958 |
| Model numbers | 71823114 |
Product
PERI-LOC VOLAR DISTAL RADIUS - RIGHT 3H STD HEAD LOCKING PLATE, 62 MM LENGTH, SST PLATE, REF 71823114, QTY: (1) NON-STERILE, Rx only, Smith & nephew, Inc., Memphis TN 38116
Reason for recall
This lot of left plates were laser etched and packaged as right plates.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2036-2017. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.