Instratek recalls
Instratek appears in 3 official U.S. recall notices indexed by RecallRadar, most recently on 2015-12-30.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
Recall summary
| Recall notices | 3 |
|---|---|
| Published | 2013-03-20 to 2015-12-30 |
| By agency | FDA Device (3) |
| By classification | Class II (3) |
| By status | terminated (3) |
| Distribution named in notices | CO, NY, TX, US, UT |
Recalls
- Hook Blade, Angled
FDA Device · Class II · 2015-12-30 · Instratek
Reason: The sterile blade will not fit into the handle provided with the ETTD system. - 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 · 2014-10-01 · Instratek
Reason: Faded and wrong markings on bone screw Countersink/Depth Gauge instruments in Mini Screw Set. - Endotrig Trigger Release Sterile Micro Hook Blade Product Usage: The blade is intended to release A-1 pulley in endoscopic trigger release…
FDA Device · Class II · 2013-03-20 · Instratek
Reason: Instratek, Inc.has received multiple complaints of the 1052 Trigger Finger Release Blades which could not be advanced into the cannula through which it is used during trigger finger release procedures.