---
title: "Bard¿ Suction Connector with ENFit, REF EN0066000 — FDA record Z-0806-2024 | 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-0806-2024-bard-suction-connector-with-enfit-ref-en0066000/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Bard¿ Suction Connector with ENFit, REF EN0066000 — FDA record Z-0806-2024

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¿ Suction Connector with ENFit, REF EN0066000
- **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**: 133610 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-0806-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0806-2024%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 00801741128707, Lot/Serial Numbers: NGFS2792, NGFS4371, NGFV1647, NGFV1669, NGGN1988, NGGN2930, NGGN3517, NGGP0451, NGGP1098, NGGV0739, NGGV2722, NGGV5069, NGGW4456, NGGX3169, NGGZ0564, NGGZ1915, NGHP2225, NGHQ2201, NGHR0090, NGHS1005, NGHS1006, NGHS2421, NGHS3331, NGHU0845, NGHU1555, NGHV0467, NGHV2758, NGHW3025, NGHX1021, NGHX3269 |

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-0806-2024%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/)