Device recall
Z-0428-2011: Penumbra System Reperfusion Catheter 032, catalog number PSC032, lot number lot…
FDA device recall · Class I · Penumbra Inc.
Key facts
| Recall number (Z-number) | Z-0428-2011 |
|---|---|
| Recall event | 57166 |
| Product | Penumbra System Reperfusion Catheter 032, catalog number PSC032, lot number lot F15020, manufactured by Penumbra, Alameda, CA. |
| Product code | NRY |
| Recalling firm | Penumbra Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jun 1, 2011 |
| 510(k) numbers | K072718 |
| FEI number | 3005168196 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
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