Device recall
Z-0018-04: Product is labeled as Cordis Pre-shaped Prowler Plus MP Infusion Catheter (3 F…
FDA device recall · Class III · Cordis Neurovascular, Inc.
Key facts
| Recall number (Z-number) | Z-0018-04 |
|---|---|
| Recall event | 26334 |
| Product | Product is labeled as Cordis Pre-shaped Prowler Plus MP Infusion Catheter (3 F proximal OD, 2.3 F Distal OD, 45 cm distal length, total length 155 cm) with an MP (45 degree) dual marker band tip. Also the package states that it is distributed by Cordis Endovascular systems, Inc, Miami, FL 33102 a… |
| Recalling firm | Cordis Neurovascular, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 11, 2004 |
| 510(k) numbers | K003925 |
| FEI number | 1000222137 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database