Codman & Shurtleff, Inc. recalls NEUROPATH 6Fx100 GUIDING CATH MPD Product Code: GMD60900000 Intended for use in the coronary, peripheral, and neurov

Recalled February 27, 2013 · FDA recall Z-0847-2013 · Codman & Shurtleff

Hazard

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

Product

NEUROPATH 6Fx100 GUIDING CATH MPD Product Code: GMD60900000 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 →