Aesculap Implant Systems LLC recalls Gomco Circumcision Clamps with separate O-Ring Component: The device is packaged non-sterile and has no shelf-life The

Recalled January 11, 2017 · FDA recall Z-0947-2017 · Aesculap Implant Systems

Hazard

Aesculap has received complaints of excessive bleeding after use of Gomco Circumcision Clamps. · FDA Class II

Units

437 units

Sold at

Nationwide Distribution

Description

Aesculap has received complaints of excessive bleeding after use of Gomco Circumcision Clamps.

Product

Gomco Circumcision Clamps with separate O-Ring Component: The device is packaged non-sterile and has no shelf-life The Gomco clamp is intended to be used for circumcision surgeries

Manufacturer(s)

Aesculap Implant Systems LLC

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →