FDA Device recall Z-1674-2015
EXPEDIUM Spine System/Synapse System
- FDA Device
- Class II
- terminated
- Published 2015-06-03
On 2015-06-03 the FDA classified a Class II recall of EXPEDIUM Spine System/Synapse System by Depuy Spine, citing device does not mate as intended.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1674-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-04-21 |
| Published | 2015-06-03 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Depuy Spine |
| Distribution | PA |
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
Device does not mate as intended.
Identifiers
| code_info | LOT NUMBER: ARNDC6 & ARN DC7 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
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FDA Device · Class II · 2019-05-08 · Depuy Spine - Concorde Lift, Expandable Interbody Device, spinal fusion implant Convex 9x21 (197809021C), 9x26 (197809026C), 11x21 (197811021C), 11x26 (1…
FDA Device · Class II · 2019-05-08 · Depuy Spine - Confidence Plus Kit Spinal Cement System, Product Codes: 283910000 (GTIN: (01)10705034209623) and 283910000 (GTIN: (01)10705034209630) The…
FDA Device · Class II · 2018-04-11 · Depuy Spine
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1674-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.