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Teleflex Medical recalls Weck Facial Closure Systems have application in laparoscopic procedures for approximation of tissues and percutaneous s
Recalled December 21, 2016 · FDA recall Z-0759-2017 · Teleflex Medical
Hazard
The devices wings may become partially detached from the EFx Shield during use. · FDA Class II
Units
2265 units
Sold at
Domestic; US Nationwide; International: Belgium, Canada.
Description
The devices wings may become partially detached from the EFx Shield during use.
Product
Weck Facial Closure Systems have application in laparoscopic procedures for approximation of tissues and percutaneous suturing for closing incision sites.
Manufacturer(s)
Teleflex Medical
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →