FDA Device recall Z-1260-2013
Mercury Spinal System DIA 5.5 x 70mm Straight Rod, Part Number: 60101-070
- FDA Device
- Class III
- terminated
- Published 2013-05-15
On 2013-05-15 the FDA classified a Class III recall of Mercury Spinal System DIA 5.5 x 70mm Straight Rod, Part Number: 60101-070 by Spinal Elements, citing spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1260-2013 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2009-04-17 |
| Published | 2013-05-15 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Spinal Elements |
| Distribution | OH, PA |
Product
Mercury Spinal System DIA 5.5 x 70mm Straight Rod, Part Number: 60101-070. Intended to provide immobilization and stabilization of the spine in skeletally mature patients.
Reason
Spinal Elements has initiated a recall for the Mercury Spinal System due to a raw material issue.
Identifiers
| code_info | Lot Number: 080596 |
|---|
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-1260-2013%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.