# FDA recall Z-1554-2021

> **Medical Action Industries, Inc. 306** · Class I · device recall initiated 2021-04-09.

## Product

Kit: CentralLineDresChangeClrSeq MAI Kit Part Number: 79420

## Reason for recall

Medical convenience kits are being recalled due to a potential breach in the package integrity  of a component, the BD ChloraPrep 3mL applicator.

## Distribution

Distributed US nationwide to OH, OR, FL and CA.

## Key facts

- **Recall number:** Z-1554-2021
- **Recalling firm:** Medical Action Industries, Inc. 306
- **Classification:** Class I
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-04-09
- **Report date:** 2021-05-19
- **Termination date:** 2023-10-03

- **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-1554-2021

## Citation

> AI Analytics. FDA recall Z-1554-2021. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-1554-2021. Source: US FDA. Licensed CC0.

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