---
title: "CardinalHealth Suction Canister Liner, MEDI-VAC CRD, REF 65651-510 — FDA record Z-0754-2024 | Is It on Recall"
description: "The above-listed lots of Cardinal Health Medi-Vac CRD\" Suction Canister Liners 1L may experience loss of suction on low or low intermittent suction settings, du"
url: https://isitonrecall.com/recall/fda-device-z-0754-2024-cardinalhealth-suction-canister-liner-medi-vac-crd-ref-65651-510/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# CardinalHealth Suction Canister Liner, MEDI-VAC CRD, REF 65651-510 — FDA record Z-0754-2024

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Dec 21, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: CardinalHealth Suction Canister Liner, MEDI-VAC CRD, REF 65651-510
- **Reason**: The above-listed lots of Cardinal Health Medi-Vac CRD" Suction Canister Liners 1L may experience loss of suction on low or low intermittent suction settings, due to a misalignment of the liner with the outer hard canister.
- **Classification**: Class II
- **Recalling firm**: Cardinal Health 200, LLC
- **Quantity**: 3505730 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0754-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0754-2024%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | UDI/DI 50630140152649 (case), Lot Numbers: J308-602, J308-605, J308-609, J308-623, J308-624, J308-625, J308-628, J308-629, J308-630, J308-632, J308-633, J308-634, J308-635, J308-636, J308-637, J308-640, J308-642, J308-607, J308-643, J309-603, J309-607, J309-623, J309-627, J309-630, J309-632, J309-635, J309-636, J309-637, J310-601, J310-609, J310-621, J310-622, J310-626, J310-627, J310-641, J310-642, J310-643, J310-644 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US, Canada, Australia and New Zealand

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Jan 24, 2024
- **Recall initiation date**: Dec 21, 2023
- **Center classification date**: Jan 18, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0754-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Cardinal Health 200, LLC records](https://isitonrecall.com/brand/cardinal-health-200-llc/)