🔍 RecallPedia

Hook Blade, Angled. Part number 7058A. Sterile disposable blade for use with Endoscopic Tarsal Tunnel Decompression (ETTD) System.

Class I - Dangerous
🏥 Medical Devices Recalled: November 24, 2015 Instratek, Incorporated Other Medical Devices

What Should You Do?

  1. Check if you have this product:
    Lot number MDHZ620
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Instratek, Incorporated
Reason for Recall:
The sterile blade will not fit into the handle provided with the ETTD system.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Hook Blade, Angled. Part number 7058A. Sterile disposable blade for use with Endoscopic Tarsal Tunnel Decompression (ETTD) System.

Product Codes/Lot Numbers:

Lot number MDHZ620

Distribution:

Distributed in: US, TX, UT, NY, CO

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0469-2016

Related Recalls