Teleflex Medical: Medical Device Recall in 2012 - (Recall #: Z-0078-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

Hem-o-lok Large Polymer Ligating Clips, REF #544240, Rx only, Sterile, Teleflex Medical, Research Triangle Park, NC 27709. Teleflex Medicals Hem-o-lok polymer ligating clips are single use, sterile, non-absorbable medial devices that have been designed to ligate vessels and tissue structures during various types of surgical procedures. Vessels and tissue structures in the range of 0.5 to 16 mm can be effectively ligated with Hem-o-lok clips.

Product Classification:

Class II

Date Initiated: September 25, 2012

Date Posted: October 24, 2012

Recall Number: Z-0078-2013

Event ID: 63365

Reason for Recall:

Product is being recalled due to the possibility that the tray may contain pinholes, compromising product sterility.

Status: Terminated

Product Quantity: 126 units

Code Information:

Catalog No. 544240, Lot #01E1200585

Distribution Pattern:

Nationwide Distribution including the state of Nevada.

Voluntary or Mandated:

Voluntary: Firm initiated