FDA Device recall Z-2679-2014
Mini Cannulated Titanium Headed and Headless Screw Set and 2.5, 3.0, and 4.0 mm countersink/depth gauges in the Mini Screw Set/System
- FDA Device
- Class II
- terminated
- Published 2014-10-01
On 2014-10-01 the FDA classified a Class II recall of Mini Cannulated Titanium Headed and Headless Screw Set and 2.5, 3.0, and 4.0 mm countersink/depth gauges in the Mini Screw Set/System by Instratek, citing faded and wrong markings on bone screw Countersink/Depth Gauge instruments in Mini Screw Set.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2679-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-04-25 |
| Published | 2014-10-01 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Instratek |
| Distribution | US |
Product
Mini Cannulated Titanium Headed and Headless Screw Set and 2.5, 3.0, and 4.0 mm countersink/depth gauges in the Mini Screw Set/System
Reason
Faded and wrong markings on bone screw Countersink/Depth Gauge instruments in Mini Screw Set.
Identifiers
| code_info | Mini System part no. IS1100 - lot 0001-0047; Instrument part nos. IS1103, IS1104, and IS1105 - lots 918101, 918102, and 918103 |
|---|
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-2679-2014%22
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