FDA Device recall Z-1664-2013
BASE, S-LIFT Instrument Case Product Usage: System cases are designed to hold and secure all instrumentation to be used with a surgical sys…
- FDA Device
- Class II
- terminated
- Published 2013-07-10
On 2013-07-10 the FDA classified a Class II recall of BASE, S-LIFT Instrument Case Product Usage: System cases are designed to hold and secure all instrumentation to be used with a surgical sys… by Spinefrontier, citing the S-LIFT Instrument Case contained a bracket with peeling nylon coating.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1664-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-05-17 |
| Published | 2013-07-10 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Spinefrontier |
| Distribution | US |
Product
BASE, S-LIFT Instrument Case Product Usage: System cases are designed to hold and secure all instrumentation to be used with a surgical system. Case and caddy components are used to contain implants intended for intervertebral body fusion and fixation of the spine.
Reason
The S-LIFT Instrument Case contained a bracket with peeling nylon coating.
Identifiers
| code_info | Lot/Serial Numbers: 7201.007 and 7201.007-1 |
|---|
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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Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1664-2013%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.