Teleflex Medical: Medical Device Recall in 2016 - (Recall #: Z-2538-2016)

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 EFx Classic Fascial Closure System, Rx Only, Sterile, The product is intended to facilitate placement and withdrawal of suture loops to repair port side defects following laparoscopic surgery

Product Classification:

Class II

Date Initiated: March 24, 2016

Date Posted: August 24, 2016

Recall Number: Z-2538-2016

Event ID: 74683

Reason for Recall:

Incorrect expiration date was printed on the product label.

Status: Terminated

Product Quantity: 45

Code Information:

Product Code EFXCT1 - Lot/Batch Nos. ML-000342, ML-000343, ML-000344, ML-000348, ML-000349; Product Code EFXSP1 - Lot/Batch Nos. ML-000345, ML-000347

Distribution Pattern:

Nationwide Distribution to CA, CO, IA, KS, MD, MI, NY, NC, PA

Voluntary or Mandated:

Voluntary: Firm initiated