6 — Class II medical device recall Z-0143-2022
Terminated recall by Smith & Nephew, Inc., reported 2021-10-27, distributed nationwide. The product label incorrectly indicated that the screws are fully threaded, but the screws contained in the pa
| Recall number | Z-0143-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Smith & Nephew, Inc., Memphis, TN, United States |
| Recall initiated | 2021-09-20 |
| Classified | 2021-10-19 |
| Reported by FDA | 2021-10-27 |
| Terminated | 2023-03-24 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 5 units |
| Reason classes | labeling |
| Lot numbers | 20GT39417 |
| Model numbers | 71106365S |
Product
6.5MMX165MM CANNULATED SCREW
Reason for recall
The product label incorrectly indicated that the screws are fully threaded, but the screws contained in the package were partially threaded.
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-0143-2022. 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.