FDA Device recall Z-0412-2013
Spine Frontier Inspan compressors Part Number: 11-60004
- FDA Device
- Class II
- terminated
- Published 2012-11-28
On 2012-11-28 the FDA classified a Class II recall of Spine Frontier Inspan compressors Part Number: 11-60004 by Spinefrontier, citing inspan Compressors may break at weld causing a loss of compression.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0412-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-08-28 |
| Published | 2012-11-28 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Spinefrontier |
| Distribution | US |
Product
Spine Frontier Inspan compressors Part Number: 11-60004. Inspan compressors provide pressure to drive spikes of Inspan implants into the spinous process bone, resulting in fixation of the implant.
Reason
Inspan Compressors may break at weld causing a loss of compression
Identifiers
| code_info | Lot Numbers: SFP02323, SFP02323R, and SFP02323RR |
|---|
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-0412-2013%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.