FDA Device recall Z-0932-2013
Cynch Lordotic T-PLlF Implant
- FDA Device
- Class II
- terminated
- Published 2013-03-20
On 2013-03-20 the FDA classified a Class II recall of Cynch Lordotic T-PLlF Implant by Spine Smith Partners, citing implants were incorrectly laser marked as 23mm instead of 28mm.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0932-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-08-24 |
| Published | 2013-03-20 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Spine Smith Partners |
| Distribution | TX |
Product
Cynch Lordotic T-PLlF Implant. Intervertebral fusion device with bone graft, for use with supplemental fixation.
Reason
Implants were incorrectly laser marked as 23mm instead of 28mm.
Identifiers
| code_info | Part Number: 0609-2809-06, Lot: 39AQ |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0932-2013%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.