Codman & Shurtleff, Inc. Recall: NEUROPATH 6Fx90 GUIDING CATH S2 Product Code: GSM60900000
Codman & Shurtleff, Inc. Recall: NEUROPATH 6Fx90 GUIDING CATH S2 Product Code: GSM60900000 is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Codman & Shurtleff, Inc.; Product: NEUROPATH 6Fx90 GUIDING CATH S2 Product Code: GSM60900000 Intended for use in the coronary, peripheral, and neur
| Recalling firm | Codman & Shurtleff, Inc. |
|---|---|
| Product | NEUROPATH 6Fx90 GUIDING CATH S2 Product Code: GSM60900000 Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices |
| Reason for recall | Sterility of device may be compromised due to lack of package integrity |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| 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 Switzerl |
| Recall initiated | 20130111 |
| Recall number | Z-0863-2013 |
| Category | device |
| State | MA |
| Country | United States |
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