Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Hook Blade Recalled by Instratek, Incorporated Due to The sterile blade will not fit into the...
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
Hook Blade, Angled. Part number 7058A. Sterile disposable blade for use with Endoscopic Tarsal Tunnel Decompression (ETTD) System.
Quantity: 39 units
Why Was This Recalled?
The sterile blade will not fit into the handle provided with the ETTD system.
Where Was This Sold?
This product was distributed to 4 states: CO, NY, TX, UT
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