Codman & Shurtleff, Inc. recalls NEUROPATH 5Fx90 GUIDING CATH HH Product Code: GHH50900000 Intended for use in the coronary, peripheral, and neurovas

Recalled February 27, 2013 · FDA recall Z-0861-2013 · Codman & Shurtleff

Hazard

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

Units

141 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 package integrity

Product

NEUROPATH 5Fx90 GUIDING CATH HH Product Code: GHH50900000 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 →