🔍 RecallPedia

Endotrig Trigger Release Sterile Micro Hook Blade Product Usage: The blade is intended to release A-1 pulley in endoscopic trigger release procedures.

Class I - Dangerous
🏥 Medical Devices Recalled: September 18, 2012 Instratek, Incorporated Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Model number 1052; Lots M674180, MAKL170, M674200
  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:
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.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Endotrig Trigger Release Sterile Micro Hook Blade Product Usage: The blade is intended to release A-1 pulley in endoscopic trigger release procedures.

Product Codes/Lot Numbers:

Model number 1052; Lots M674180, MAKL170, M674200

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0922-2013

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