# FDA recall Z-1787-2021

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

## Product

DIALYSIS ACCESS Medical convenience kit,  Avid Medical Part Number: VMED004-03.

## 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.  Under certain circumstances the applicator may grow Aspergillus penicillioides, which may result in a breach of the package integrity. A breach of package integrity may contaminate other components in AVID Medical kits.

## Distribution

Distributed US nationwide to TX, AZ, IL, MS, LA, MO, and TN

## Key facts

- **Recall number:** Z-1787-2021
- **Recalling firm:** Avid Medical, Inc.
- **Classification:** Class I
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-04-09
- **Report date:** 2021-06-16
- **Termination date:** 2022-07-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Toano, VA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1787-2021

## Citation

> AI Analytics. FDA recall Z-1787-2021. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1787-2021. Source: US FDA. Licensed CC0.

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