TITANIUM END CAP WITH T40 STARDRIVE RECESS — Class II medical device recall Z-2051-2015
Terminated recall by Synthes, Inc., reported 2015-07-15, distributed in MO, SC. A specific part and lot number was packaged and shipped prior to the completion of a required internal inspect
| Recall number | Z-2051-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Synthes, Inc., West Chester, PA, United States |
| Recall initiated | 2015-06-03 |
| Classified | 2015-07-08 |
| Reported by FDA | 2015-07-15 |
| Terminated | 2015-09-15 |
| Distributed | MO, SC |
| Quantity | 3 |
| Lot numbers | 7950994 |
| Model numbers | 04.004.000 |
Product
TITANIUM END CAP WITH T40 STARDRIVE RECESS, 0MM EXTENSION FOR TITANIUM TIBIAL NAILS-EX; Synthes Tibial Nail System EX is intended to stabilize fractures of the proximal and distal tibia and the tibial shaft; open and closed tibial shaft fractures; certain pre-and post-isthmic fractures; and tibial malunions and non-unions.
Reason for recall
A specific part and lot number was packaged and shipped prior to the completion of a required internal inspection.
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-2051-2015. 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.