Reported Mar 20, 2013 · Terminated

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

Instratek, Incorporated

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Instratek, Incorporated · 4141 Directors Row · Houston, TX · 77092-8743

Is this the product you have?

  • Endotrig Trigger Release
  • Sterile Micro Hook Blade Product UsageThe blade is intended to release A-1 pulley in endoscopic trigger release procedures
Lot codes and dates
    • Model number 1052
    • Lots M674180
    • MAKL170
    • M674200
Amount recalled
235

Where it was sold

Why it was recalled

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.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Apr 10, 2013 · Data as of Sep 19, 5:35 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.