FDA Device recall Z-0576-2014
Indus Invue Screws: IM71013-XX: Indus Screw04.0mm SelfDrilling
- FDA Device
- Class II
- terminated
- Published 2014-01-01
On 2014-01-01 the FDA classified a Class II recall of Indus Invue Screws: IM71013-XX: Indus Screw04.0mm SelfDrilling by Spinefrontier, citing mismarked and unmarked screws.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0576-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-11-20 |
| Published | 2014-01-01 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Spinefrontier |
| Distribution | US |
Product
Indus Invue Screws: IM71013-XX: Indus Screw04.0mm SelfDrilling. Used to secure the Invue Anterior Cervical Plate in position.
Reason
Mismarked and unmarked screws
Identifiers
| code_info | Lot/Serial Number: IM71013-01: Lot 0000 |
|---|
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-0576-2014%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.