# FDA recall Z-0806-2024

> **C.R. Bard Inc** · Class II · device recall initiated 2023-12-20.

## Product

Bard¿ Suction Connector with ENFit, REF EN0066000

## Reason for recall

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.

## Distribution

US

## Key facts

- **Recall number:** Z-0806-2024
- **Recalling firm:** C.R. Bard Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-12-20
- **Report date:** 2024-01-31

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Covington, GA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0806-2024

## Citation

> AI Analytics. FDA recall Z-0806-2024. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/Z-0806-2024. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*