Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Mini Cannulated Titanium Headed and Headless Screw Set and 2.5 Recalled by Instratek, Incorporated Due to Faded and wrong markings on bone screw Countersink/Depth...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Instratek, Incorporated directly.
Affected Products
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
Quantity: 96
Why Was This Recalled?
Faded and wrong markings on bone screw Countersink/Depth Gauge instruments in Mini Screw Set.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Instratek, Incorporated
Instratek, Incorporated has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report