| | Class 2 Recall Codman (and Formerly MICRUS) NEUROPATH |  |
| Date Posted |
February 20, 2013 |
| Recall Number |
Z-0855-2013 |
| Product |
NEUROPATH 5Fx90 GUIDING CATH MPC
Product Code: GMC50900000
Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices |
| Code Information |
All unexpired lots
|
Recalling Firm/ Manufacturer |
Codman & Shurtleff, Inc. 325 Paramount Drive Raynham, Massachusetts 02767 |
| Consumer Instructions |
No consumer action necessary |
Reason for Recall |
Sterility of device may be compromised due to lack of package integrity
|
| Action |
Codman sent an Urgent Voluntary Product Recall Notification letter dated January 11, 2013, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were advised to check all inventory to determine if they have any affected product, use the included instructions to report inventory status, return and obtain replacement product. Customers were instructed to contact your local Codman Representative or Stericycle at 1-866-201-9077.
For questions regarding this recall call 508-880-8100. |
| Quantity in Commerce |
202 units |
| Distribution |
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. |
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