Device recall
Z-1391-2011: Haemonetics cardioPAT Cardiovascular - autotransfusion System Catalog Number…
FDA device recall · Class II · Haemonetics Corporation
Key facts
| Recall number (Z-number) | Z-1391-2011 |
|---|---|
| Recall event | 57805 |
| Product | Haemonetics cardioPAT Cardiovascular - autotransfusion System Catalog Number: 02050-US |
| Product code | CAC |
| Recalling firm | Haemonetics Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 14, 2013 |
| 510(k) numbers | K053000 |
| FEI number | 1219343 |
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