Home › Device types › FIR
Pump, Blood, Extra-Luminal
FDA product code FIR · Class 2 · Gastroenterology, Urology
0
Registered devices
8
Adverse events
3
Recalls
7
510(k) clearances
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2012-07-09 | Apheresis Technologies, Inc. | On 07/09/2012, Apheresis Technologies, Inc. initiated a recall on the Plasma Pump Model PP-04a due to a complaint received regarding a rotor of the PP-04a pump |
| 2010-11-29 | Apheresis Technologies, Inc. | Apheresis Technologies, Inc., Palm Harbor, FL, initiated a voluntarily withdrawal on November 29, 2010 of their five (5) units of the Plasma Pro Plasma Pump and |
| 2009-04-01 | Apheresis Technologies, Inc. | Apheresis Technologies, Inc. is taking the following Corrective Action: Modification of the Owners Manual Only for the PlasmaPro Plasma Pump Model PP-05. Oper |
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