Apheresis Technologies, Inc.: Medical Device Recall in 2012 - (Recall #: Z-2149-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

Plasma Pump Model PP-04a Used with Asahi Plasmaflo Plasma Separators and plasma exchange tubesets to perform therapeutic plasma exchange.

Product Classification:

Class II

Date Initiated: July 9, 2012

Date Posted: August 15, 2012

Recall Number: Z-2149-2012

Event ID: 62563

Reason for Recall:

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 that stopped during a therapeutic plasma exchange treatment causing interruption of flow of both the plasma discard line and replacement fruit line.

Status: Terminated

Product Quantity: 13

Code Information:

D11003544 through D11003552 D11003556 through D11003558

Distribution Pattern:

Natonwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated