---
title: "Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx On... — FDA record Z-2007-2026 | Is It on Recall"
description: "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 sy"
url: https://isitonrecall.com/recall/fda-device-z-2007-2026-medical-action-industries-inc-pack-cath-bhh-ref-bhca49k-sterile-eo-rx-only-qty-5-case/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case — FDA record Z-2007-2026

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 Mar 17, 2026. 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**: Medical Action Industries Inc. Pack Cath BHH, REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case
- **Reason**: 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"
- **Classification**: Class I
- **Recalling firm**: Medical Action Industries, Inc. 306
- **Quantity**: 2030 kits
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2007-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2007-2026%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:20809160490294/ Lot numbers: 342509, 346066, 338434, 339423, 337365, 335489, 336189, 336789 |

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

## Distribution

US distribution to state of: AZ OUS: None

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Arizona](https://isitonrecall.com/state/arizona/)

## Dates in the source

- **Report date**: May 13, 2026
- **Recall initiation date**: Mar 17, 2026
- **Center classification date**: May 6, 2026

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-2007-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Medical Action Industries, Inc. 306 records](https://isitonrecall.com/brand/medical-action-industries-inc-306/)