# FDA recall Z-1550-2020

> **Carroll-Baccari, Inc.** · Class II · device recall initiated 2019-12-23.

## Product

MVAP MEDICAL SUPPLIES INC, Mavidon CardioPrep Single, 24 use cups, Re order #  MCP-24

## Reason for recall

Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug Administration inspection on October 15, 2019 were tested and found to be contaminated with Burkholderia cepacia. Mavidon is recalling all products manufactured at their facility.

## Distribution

Nationwide, Canada, UK, Spain, Australia

## Key facts

- **Recall number:** Z-1550-2020
- **Recalling firm:** Carroll-Baccari, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-12-23
- **Report date:** 2020-04-01
- **Termination date:** 2021-09-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Riviera Beach, FL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1550-2020

## Citation

> AI Analytics. FDA recall Z-1550-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1550-2020. Source: US FDA. Licensed CC0.

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