Indus Invue Screws: IM71058-XX: 04 — Class II medical device recall Z-0573-2014
Terminated recall by SpineFrontier, Inc., reported 2014-01-01, distributed nationwide. Mismarked and unmarked screws
| Recall number | Z-0573-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | SpineFrontier, Inc., Beverly, MA, United States |
| Recall initiated | 2013-11-20 |
| Classified | 2013-12-26 |
| Reported by FDA | 2014-01-01 |
| Terminated | 2018-09-06 |
| Distributed | Nationwide (US) |
| Quantity | 993 |
| Lot numbers | 0000, IM71058-02, IM71058-03 |
| Serial numbers | IM71058-0L |
Product
Indus Invue Screws: IM71058-XX: 04.2mm, SelfTapping, Tapered. Used to secure the Invue Anterior Cervical Plate in position.
Reason for recall
Mismarked and unmarked screws
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-0573-2014. 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.