Cardinal Health, Medical Products & Services: Medical Device Recall in 2013 - (Recall #: Z-1199-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Presource PBDS, Hand, Kit, Circulator

Product Classification:

Class I

Date Initiated: March 26, 2013

Date Posted: May 15, 2013

Recall Number: Z-1199-2013

Event ID: 64736

Reason for Recall:

Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit that may contain outer plastic packaging on one or more components. If the packaging is removed without disassembling the components, remnants of the plastic from the packaging material may become lodged in the filter potentially causing an obstruction of airflow.

Status: Terminated

Product Quantity: 4,571 Kits total

Code Information:

Catalog Number: PO24HKGWG01; Lots: 856515, 875680, 894983, 905021, 929987, 932368, 946822, 954543, 968547

Distribution Pattern:

Distributed in the states of AR, MS, SC, and TN.

Voluntary or Mandated:

Voluntary: Firm initiated