Instratek, Incorporated: Medical Device Recall in 2013 - (Recall #: Z-0922-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product 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 Classification:

Class II

Date Initiated: September 18, 2012

Date Posted: March 20, 2013

Recall Number: Z-0922-2013

Event ID: 63551

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.

Status: Terminated

Product Quantity: 235

Code Information:

Model number 1052; Lots M674180, MAKL170, M674200

Distribution Pattern:

USA Nationwide Distribution including the states of: AZ, MI, NE, NV, and TX.

Voluntary or Mandated:

Voluntary: Firm initiated