# FDA recall Z-0751-2023

> **Medical Action Industries, Inc. 306** · Class II · device recall initiated 2022-11-04.

## Product

Medical Action INDUSTRIES INC. Port a Cath Kit REF 58647D, cardiac catheter introduction kit

## Reason for recall

XXX

## Distribution

US Nationwide distribution in the state of VA.

## Key facts

- **Recall number:** Z-0751-2023
- **Recalling firm:** Medical Action Industries, Inc. 306
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-11-04
- **Report date:** 2022-12-28
- **Termination date:** 2026-03-18

- **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-0751-2023

## Citation

> AI Analytics. FDA recall Z-0751-2023. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0751-2023. Source: US FDA. Licensed CC0.

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