# FDA recall Z-2007-2026

> **Medical Action Industries, Inc. 306** · Class I · device recall initiated 2026-03-17.

## Product

Medical Action Industries Inc.   Pack Cath BHH,   REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case

## Reason for recall

Convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between the syringe and manifold"

## Distribution

US distribution to state of: AZ OUS: None

## Key facts

- **Recall number:** Z-2007-2026
- **Recalling firm:** Medical Action Industries, Inc. 306
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-03-17
- **Report date:** 2026-05-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Arden, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2007-2026

## Citation

> AI Analytics. FDA recall Z-2007-2026. Retrieved 2026-07-03 from https://api.ai-analytics.org/recall/Z-2007-2026. Source: US FDA. Licensed CC0.

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