---
title: "Bard¿ PreVent¿ Anti-Reflux Filter with ENFit, REF EN0046000 — FDA record Z-0795-2024 | Is It on Recall"
description: "BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompressi"
url: https://isitonrecall.com/recall/fda-device-z-0795-2024-bard-prevent-anti-reflux-filter-with-enfit-ref-en0046000/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Bard¿ PreVent¿ Anti-Reflux Filter with ENFit, REF EN0046000 — FDA record Z-0795-2024

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 20, 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**: Bard¿ PreVent¿ Anti-Reflux Filter with ENFit, REF EN0046000
- **Reason**: BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.
- **Classification**: Class II
- **Recalling firm**: C.R. Bard Inc
- **Quantity**: 39430 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0795-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0795-2024%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 00801741113765, Lot/Serial Numbers: NGEV2409, NGEY1492, NGEY2717, NGEZ0908, NGEZ1657, NGEZ2692, NGFQ4105, NGFR1077, NGFR2312, NGFR3259, NGFS1627, NGFS4431, NGFT5468, NGFU1877, NGFU3837, NGFV1652, NGFV3513, NGFW1856, NGFX0167, NGFX2672, NGFX5611, NGGP3169, NGGT3611 |

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

## Distribution

US

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

## Dates in the source

- **Report date**: Jan 31, 2024
- **Recall initiation date**: Dec 20, 2023
- **Center classification date**: Jan 25, 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-0795-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [C.R. Bard Inc records](https://isitonrecall.com/brand/c-r-bard-inc/)