Device recall
Z-1654-2012: PlasmaPrO" Plasma Pump Model PP-05 Product Usage: The PlasmaPro Plasma Pump is a…
FDA device recall · Class II · Apheresis Technologies, Inc.
Key facts
| Recall number (Z-number) | Z-1654-2012 |
|---|---|
| Recall event | 61621 |
| Product | PlasmaPrO" Plasma Pump Model PP-05 Product Usage: The PlasmaPro Plasma Pump is a pump to be used with Asahi Plasma Separators to perform therapeutic plasma exchange. |
| Product code | FIR |
| Recalling firm | Apheresis Technologies, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 25, 2012 |
| FEI number | 1000113717 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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