Teleflex Medical: Medical Device Recall in 2016 - (Recall #: Z-0759-2017)

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 Facial Closure Systems have application in laparoscopic procedures for approximation of tissues and percutaneous suturing for closing incision sites.

Product Classification:

Class II

Date Initiated: November 16, 2016

Date Posted: December 21, 2016

Recall Number: Z-0759-2017

Event ID: 75693

Reason for Recall:

The devices wings may become partially detached from the EFx Shield during use.

Status: Terminated

Product Quantity: 2265 units

Code Information:

Product Code: EFX002, Lot numbers: 3264480000, 3269990000, 3270100000.

Distribution Pattern:

Domestic; US Nationwide; International: Belgium, Canada.

Voluntary or Mandated:

Voluntary: Firm initiated