Device recall
Z-2149-2012: Plasma Pump Model PP-04a Used with Asahi Plasmaflo Plasma Separators and plasma…
FDA device recall · Class II · Apheresis Technologies, Inc.
Key facts
| Recall number (Z-number) | Z-2149-2012 |
|---|---|
| Recall event | 62563 |
| Product | Plasma Pump Model PP-04a Used with Asahi Plasmaflo Plasma Separators and plasma exchange tubesets to perform therapeutic plasma exchange. |
| Product code | FIR |
| Recalling firm | Apheresis Technologies, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 16, 2013 |
| 510(k) numbers | K961137 |
| FEI number | 1000113717 |
At a glance
- 1–9 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