EXPEDIUM Spine System/Synapse System — Class II medical device recall Z-1674-2015
Terminated recall by DePuy Spine, Inc., reported 2015-06-03. Device does not mate as intended.
| Recall number | Z-1674-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | DePuy Spine, Inc., Raynham, MA, United States |
| Recall initiated | 2015-04-21 |
| Classified | 2015-05-26 |
| Reported by FDA | 2015-06-03 |
| Terminated | 2018-10-03 |
| Quantity | 183 devices |
| UPC / GTIN / UDI-DI | 10705034032467 |
| Lot numbers | ARNDC6, DC7 |
| Model numbers | 1754-91-150 |
Product
EXPEDIUM Spine System/Synapse System; MODEL: EXPEDIUM Offset Conical Lock Nut 8mm, CATALOG NO. : 1754-91-150, UDI NUMBER (if applicable): GTIN: 10705034032467
Reason for recall
Device does not mate as intended.
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-1674-2015. 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.