FDA Device recall Z-0849-2018
Concorde Lift Torque Limiting Handle
- FDA Device
- Class II
- terminated
- Published 2018-03-14
On 2018-03-14 the FDA classified a Class II recall of Concorde Lift Torque Limiting Handle by Depuy Orthopaedics, citing potential for Intra-operative breakage of driver tips.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0849-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-07-26 |
| Published | 2018-03-14 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Depuy Orthopaedics |
| Distribution | US |
Product
Concorde Lift Torque Limiting Handle. Must be used with supplemental internal spinal fixation systems that have been cleared for use in the lumbar spine.
Reason
Potential for Intra-operative breakage of driver tips
Identifiers
| code_info | Product code: 287804102 Lot number: 122315-B R, 122315-A R, 041117A |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0849-2018%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.