Presource PBDS — Class I medical device recall Z-1200-2013
Terminated recall by Cardinal Health, Medical Products & Services, reported 2013-05-15, distributed in AR, MS, SC, TN. Various Presource Kits contain a pre-assembled Filter and Anesthesia Circuit that may contain outer plastic pa
| Recall number | Z-1200-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cardinal Health, Medical Products & Services, Park City, IL, United States |
| Recall initiated | 2013-03-26 |
| Classified | 2013-05-03 |
| Reported by FDA | 2013-05-15 |
| Terminated | 2017-04-12 |
| Distributed | AR, MS, SC, TN |
| Quantity | 4,571 kits |
| Lot numbers | 847129, 877843, 905183, 931801, 935180, 946651, 957422, 969585 |
| Model numbers | PO24SAGWF01 |
Product
Presource PBDS, Shoulder Arthroscopy, Kit, Circulator
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1200-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.