Instratek, Incorporated recalls
Instratek, Incorporated has 3 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 30 Dec 2015. The most frequent reason is sterility.
Total recalls3since 2013
Last 12 months0reported
Class I00% of total
Ongoing0latest 30 Dec 2015
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 3 100%Class III 0 0%
Why instratek, incorporated is recalled
Product types
By year
All instratek, incorporated recalls, newest first
3 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Hook Blade, Angled recalled by Instratek, Incorporated | Instratek, Incorporated | Sterility | 4 states |
| Device | CLASS II | Mini Cannulated Titanium Headed and Headless Screw Set recalled | Instratek, Incorporated | Other | Nationwide |
| Device | CLASS II | Endotrig Trigger Release Sterile Micro Hook Blade recalled | Instratek, Incorporated | Sterility | Nationwide |
About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.