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Teleflex Medical recalls Weck EFx Classic Fascial Closure System, Rx Only, Sterile, The product is intended to facilitate placement and withdr
Recalled August 24, 2016 · FDA recall Z-2538-2016 · Teleflex Medical
Hazard
Incorrect expiration date was printed on the product label. · FDA Class II
Units
45
Sold at
Nationwide Distribution to CA, CO, IA, KS, MD, MI, NY, NC, PA
Description
Incorrect expiration date was printed on the product label.
Product
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
Manufacturer(s)
Teleflex Medical
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →