Teleflex Medical: Medical Device Recall in 2016 - (Recall #: Z-2759-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

WECK¿ Horizon" Manual-Load Ligating Clip Applier, For Medium-Large Size Horizon Ligation Clips Curved Jaw, 11 (28cm), Rx Only, REF 337111, Product Usage: Weck Closure Systems applier has been designed and calibrated for use with specific Horizon, Hemoclip Plus Hemoclip Traditional, or Atrauclip ligating clips as indicated. Applier color coding matches the color of the ligating clip cartridge for which it is to be used. Hemoclip Plus appliers are easily identified by one black-ring handle.

Product Classification:

Class II

Date Initiated: August 24, 2016

Date Posted: September 14, 2016

Recall Number: Z-2759-2016

Event ID: 75020

Reason for Recall:

Misbranded: Incorrect etching on the device.

Status: Terminated

Product Quantity: 49 units

Code Information:

Product Code: 337111, Lot Number: 06F1515745.

Distribution Pattern:

Worldwide Distribution US Nationwide in the states of FL, IL, KY, MI, NY and OK and countries of Mexico and Canada.

Voluntary or Mandated:

Voluntary: Firm initiated