META-TAN LAG/COMPRESSION SCREW KIT 90MM/85MM — Class II medical device recall Z-1806-2025
Ongoing recall by Smith & Nephew, Inc., reported 2025-05-28, distributed nationwide. Integrated Lag/Compression Screw Kit has a compression screw with hexagon socket that may be undersized, which
| Recall number | Z-1806-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Smith & Nephew, Inc., Memphis, TN, United States |
| Recall initiated | 2025-03-18 |
| Classified | 2025-05-19 |
| Reported by FDA | 2025-05-28 |
| Distributed | Nationwide (US) |
| Quantity | 75 |
| UPC / GTIN / UDI-DI | 00885556132975 |
| Lot numbers | 24CT81426 |
| Model numbers | 71642690 |
| Expiration dates | 2034-03-25 |
Product
META-TAN LAG/COMPRESSION SCREW KIT 90MM/85MM, REF: 71642690
Reason for recall
Integrated Lag/Compression Screw Kit has a compression screw with hexagon socket that may be undersized, which causes the screw to be non-functional, which would require replacement with another adequate size screw, and exchange may exceed 30 minutes.
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-1806-2025. 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.