FDA Device recall Z-1199-2013
Presource PBDS, Hand, Kit, Circulator
- FDA Device
- Class I
- terminated
- Published 2013-05-15
On 2013-05-15 the FDA classified a Class I recall of Presource PBDS, Hand, Kit, Circulator by Cardinal Health Medical Products And Services, citing 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 withou….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1199-2013 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2013-03-26 |
| Published | 2013-05-15 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Cardinal Health Medical Products And Services |
| Distribution | AR, MS, SC, TN |
Product
Presource PBDS, Hand, Kit, Circulator
Reason
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.
Identifiers
| code_info | Catalog Number: PO24HKGWG01; Lots: 856515, 875680, 894983, 905021, 929987, 932368, 946822, 954543, 968547 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1199-2013%22
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