DIAMOND POINT — Class II medical device recall Z-3172-2024
Ongoing recall by Smith & Nephew, Inc., reported 2024-09-25. Smith & Nephew, Inc., has initiated a field action to voluntarily remove two batches of K-Wires due to a packa
| Recall number | Z-3172-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Smith & Nephew, Inc., Memphis, TN, United States |
| Recall initiated | 2024-07-09 |
| Classified | 2024-09-19 |
| Reported by FDA | 2024-09-25 |
| Countries outside the US | CA, NO |
| Quantity | 73 units |
| Reason classes | labeling |
| Lot numbers | 21KNX0074 |
| Model numbers | 128062 |
Product
DIAMOND POINT, BOTH ENDS K-WIRE, REF 128062, metallic bone fixation fastener
Reason for recall
Smith & Nephew, Inc., has initiated a field action to voluntarily remove two batches of K-Wires due to a packaging error. A complaint was received indicating that a package contained K-WIRE .062X9 2PT DM wires instead of K-WIRE .045X9 2PT DM as described on the product label.
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-3172-2024. 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.