US Endoscopy Group Inc: Medical Device Recall in 2015 - (Recall #: Z-0001-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Histolock Resection Device, US Endoscopy. An electrosurgical device designed to be used to endoscopically grasp, dissect and transect tissue during gastrointestinal endoscopic procedures.

Product Classification:

Class II

Date Initiated: July 14, 2015

Date Posted: October 7, 2015

Recall Number: Z-0001-2016

Event ID: 71987

Reason for Recall:

The company has determined the sterility cannot be assured for the affected lot.

Status: Terminated

Product Quantity: 41 units

Code Information:

M/N: 00711117; Lot #: 1505956

Distribution Pattern:

US Distribution to states of: AL, AR, CA, IL, IN, MS, OH, OK & TN.

Voluntary or Mandated:

Voluntary: Firm initiated