Teleflex Medical: Medical Device Recall in 2014 - (Recall #: Z-0771-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

Weck, Electrosurgical Coagulation Suction Tube 8 (20.0cm), 11 French, with Stylet, Teleflex Medical, Research Triangle, NC 27709. Intended to remove tissue and control bleeding by use of high-frequency electrical current.

Product Classification:

Class II

Date Initiated: December 19, 2013

Date Posted: January 22, 2014

Recall Number: Z-0771-2014

Event ID: 67129

Reason for Recall:

Sterility cannot be guaranteed.

Status: Terminated

Product Quantity: 17,450 ea

Code Information:

Catalog Number: 809610, Lot Number: 01A1100610.

Distribution Pattern:

Nationwide Distribution.

Voluntary or Mandated:

Voluntary: Firm initiated