Teleflex Medical: Medical Device Recall in 2017 - (Recall #: Z-2108-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

WECK Visistat 35R Disposable Skin Stapler, Ref 528135, Rx Only, Sterile EO, Visistat is indicated for the external skin closure of lacerations on the outer layer of the dermis for a wide range of general, thoracic, obstetric, gynecological, orthopedic, cardiovascular, urological, and plastic surgical procedures

Product Classification:

Class II

Date Initiated: March 24, 2017

Date Posted: May 24, 2017

Recall Number: Z-2108-2017

Event ID: 77102

Reason for Recall:

Some boxes are labeled as containing Visistat Wide devices, when they in fact they contained Visistat Regular device.

Status: Completed

Product Quantity: 3594 eaches

Code Information:

73H1600207

Distribution Pattern:

Worldwide Distribution - US including CA, FL, GA, IL, IN, KS, KY, ME, MD, MA, MI, NJ, NY, NC, OH, OR, RI, TX, UT, VA, and Internationally to Australia, Belgium and France

Voluntary or Mandated:

Voluntary: Firm initiated