Synthes 2 — Class II medical device recall Z-0406-2014
Terminated recall by Synthes (USA) Products LLC, reported 2013-12-04, distributed nationwide. A complaint was reported regarding a screw being found in a package labeled for 2.4 mm LC-DCP Plate.
| Recall number | Z-0406-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Synthes (USA) Products LLC, West Chester, PA, United States |
| Recall initiated | 2013-07-30 |
| Classified | 2013-11-26 |
| Reported by FDA | 2013-12-04 |
| Terminated | 2015-08-17 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 13 |
| Reason classes | labeling |
| Lot numbers | 8093100 |
| Model numbers | 249.926 |
Product
Synthes 2.4 mm LC-DCP Plate 6 Holes/51mm Product Usage: Intended for fractures, osteotomies, and replantations of small bones including the foot, ankle, and hand.
Reason for recall
A complaint was reported regarding a screw being found in a package labeled for 2.4 mm LC-DCP Plate.
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-0406-2014. 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.