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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 64736

14 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
March 26, 2013
Product types
Device
Classifications
Class I
Statuses
Terminated
Recalling firm wording
Cardinal Health, Medical Products & Services

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

14 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 14

Presource PBDS, Gyn Laparoscopy Kit, Circulator

Z-1193-2013
Recall number
Z-1193-2013
Initiated
March 26, 2013
Classification
Class I
Status
Terminated
Quantity
4,571 Kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging process control

Compare all device evidence states

Inspect official wording and provenance

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.

Code information

Catalog Number: PB24LSNPC01; Lots: 152737, 159630, 168459, 176674, 187217, 197319, 840618

Distribution pattern

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

device · product 2 of 14

A) Presource PBDS, Lap Chole, Kit, Clean Up; B) Presource PBDS, Greenwood LeFlore Hosp, Lap Chole, Kit

Z-1194-2013
Recall number
Z-1194-2013
Initiated
March 26, 2013
Classification
Class I
Status
Terminated
Quantity
4,571 Kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging process control

Compare all device evidence states

Inspect official wording and provenance

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.

Code information

A) Catalog Number: PG24LCGWG02; Lots: 153502, 162892, 170494, 180482, , 88701, 193548, 198163, 206986; B) Catalog Number: PG24LCGWG; Lots:153502, 162892, 170494, 180482, 188701, 193548, 198163, 206986

Distribution pattern

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

device · product 3 of 14

Presource PBDS, General Laparoscopy, Kit, Circulator

Z-1195-2013
Recall number
Z-1195-2013
Initiated
March 26, 2013
Classification
Class I
Status
Terminated
Quantity
4,571 Kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging process control

Compare all device evidence states

Inspect official wording and provenance

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.

Code information

Catalog Number: PG24LGNPC01; Lots: 147492, 152554, 160275, 165822, 173745, 180700, 186904, 195042, 205901, 836989

Distribution pattern

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

device · product 4 of 14

Presource PBDS, Major Abdominal, Kit, Circulator

Z-1196-2013
Recall number
Z-1196-2013
Initiated
March 26, 2013
Classification
Class I
Status
Terminated
Quantity
4,571 Kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging process control

Compare all device evidence states

Inspect official wording and provenance

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.

Code information

Catalog Number: PG24MANPC01; Lots: 840143, 857320, 871000, 882315, 900599, 928133, 942238, 952387, 964048

Distribution pattern

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

device · product 5 of 14

Presource PBDS, Knee Arthroscopy, Kit, Circulator

Z-1197-2013
Recall number
Z-1197-2013
Initiated
March 26, 2013
Classification
Class I
Status
Terminated
Quantity
4,571 Kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging process control

Compare all device evidence states

Inspect official wording and provenance

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.

Code information

Catalog Number: PO24AKNPC01; Lots: 851288, 877594, 901672, 917786, 948443, 972424

Distribution pattern

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

device · product 6 of 14

Presource PBDS, Extremity, Kit, Circulator

Z-1198-2013
Recall number
Z-1198-2013
Initiated
March 26, 2013
Classification
Class I
Status
Terminated
Quantity
4,571 Kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging process control

Compare all device evidence states

Inspect official wording and provenance

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.

Code information

Catalog Number: PO24EXNPD01; Lots: 852429, 868825, 883022, 896400, 914524, 929984, 941696, 954317

Distribution pattern

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

device · product 7 of 14

Presource PBDS, Hand, Kit, Circulator

Z-1199-2013
Recall number
Z-1199-2013
Initiated
March 26, 2013
Classification
Class I
Status
Terminated
Quantity
4,571 Kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging process control

Compare all device evidence states

Inspect official wording and provenance

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.

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.

device · product 8 of 14

Presource PBDS, Shoulder Arthroscopy, Kit, Circulator

Z-1200-2013
Recall number
Z-1200-2013
Initiated
March 26, 2013
Classification
Class I
Status
Terminated
Quantity
4,571 Kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging process control

Compare all device evidence states

Inspect official wording and provenance

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.

Code information

Catalog Number: PO24SAGWF01; Lots: 847129, 877843, 905183, 931801, 935180, 946651, 957422, 969585

Distribution pattern

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

device · product 9 of 14

Presource PBDS, Shoulder Procedure, Kit, Circulator

Z-1201-2013
Recall number
Z-1201-2013
Initiated
March 26, 2013
Classification
Class I
Status
Terminated
Quantity
4,571 Kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging process control

Compare all device evidence states

Inspect official wording and provenance

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.

Code information

Catalog Number: PO24SHNPC01; Lots: 843685, 864636, 875004, 893118, 901720, 924132, 934399, 959120, 968668

Distribution pattern

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

device · product 10 of 14

Presource PBDS, Total Hip, Kit, Circulator

Z-1202-2013
Recall number
Z-1202-2013
Initiated
March 26, 2013
Classification
Class I
Status
Terminated
Quantity
4,571 Kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging process control

Compare all device evidence states

Inspect official wording and provenance

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.

Code information

Catalog Number: PO24THGWG01; Lots: 966051, 970753

Distribution pattern

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

device · product 11 of 14

Presource PBDS, Total Joint, Kit, Circulator

Z-1203-2013
Recall number
Z-1203-2013
Initiated
March 26, 2013
Classification
Class I
Status
Terminated
Quantity
4,571 Kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging process control

Compare all device evidence states

Inspect official wording and provenance

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.

Code information

Catalog Number: PO24TJNPC01; Lots: 843134, 851291, 875033, 893475, 911751, 914529, 928726, 948543, 968125,

Distribution pattern

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

device · product 12 of 14

Presource PBDS, Total Knee, Kit, Circulator

Z-1204-2013
Recall number
Z-1204-2013
Initiated
March 26, 2013
Classification
Class I
Status
Terminated
Quantity
4,571 Kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging process control

Compare all device evidence states

Inspect official wording and provenance

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.

Code information

Catalog Number: PO24TKGWE01; Lots: 828654, 851596, 872322, 879459, 885132, 905305, 920462, 934298, 946652, 959208

Distribution pattern

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

device · product 13 of 14

Presource PBDS, Beaufort Memorial Hospital, Anesthesia Circuit, Kit

Z-1205-2013
Recall number
Z-1205-2013
Initiated
March 26, 2013
Classification
Class I
Status
Terminated
Quantity
4,571 Kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging process control

Compare all device evidence states

Inspect official wording and provenance

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.

Code information

Catalog Number:PZ23ANBUG; Lot: 200710

Distribution pattern

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

device · product 14 of 14

Presource PBDS, Knee Arthroscopy, Kit, Circulator

Z-1206-2013
Recall number
Z-1206-2013
Initiated
March 26, 2013
Classification
Class I
Status
Terminated
Quantity
4,571 Kits total

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Packaging process control

Compare all device evidence states

Inspect official wording and provenance

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.

Code information

Catalog Number: PO24KAGWE01; Lots: 839276, 851503, 884374, 905171, 930617, 946381, 952446, 959782

Distribution pattern

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

Field note

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