Codman & Shurtleff, Inc. recalls NEUROPATH 6Fx90 GUIDING CATH MPC Product Code: GMC60900000 Intended for use in the coronary, peripheral, and neurova

Recalled February 27, 2013 · FDA recall Z-0842-2013 · Codman & Shurtleff

Hazard

Sterility of device may be compromised due to lack of packaging integrity · FDA Class II

Units

867 units

Sold at

Worldwide Distribution - USA (nationwide) and Internationally to Austria, Belgium, Canada, Chile, Costa, Rica, Czech Republic, Denmark, France, Germany, Great Britian/UK, Ireland, Italy, Lithuania, Malaysia, Netherlands, New Zealand, Norway, Poland, Portugal, Singapore, Slovakia, Spain, and Switzerland.

Description

Sterility of device may be compromised due to lack of packaging integrity

Product

NEUROPATH 6Fx90 GUIDING CATH MPC Product Code: GMC60900000 Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices

Manufacturer(s)

Codman & Shurtleff, Inc.

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