BASE — Class II medical device recall Z-1664-2013
Terminated recall by SpineFrontier, Inc., reported 2013-07-10, distributed nationwide. The S-LIFT Instrument Case contained a bracket with peeling nylon coating.
| Recall number | Z-1664-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | SpineFrontier, Inc., Beverly, MA, United States |
| Recall initiated | 2013-05-17 |
| Classified | 2013-07-04 |
| Reported by FDA | 2013-07-10 |
| Terminated | 2016-05-17 |
| Distributed | Nationwide (US) |
| Quantity | 12 |
| Serial numbers | 7201.007, 7201.007-1 |
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 for recall
The S-LIFT Instrument Case contained a bracket with peeling nylon coating.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1664-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.