# FDA recall Z-2075-2020

> **Becton Dickinson & Company** · Class II · device recall initiated 2020-02-26.

## Product

BARD MYPICC KIT 5F Dual-Lumen, Catalog Number CK000025

## Reason for recall

The kits contain surgical gowns which were subject to a recall by the supplier.

## Distribution

The products were distributed to the following US states: IN, MO, OH, and TX.

## Key facts

- **Recall number:** Z-2075-2020
- **Recalling firm:** Becton Dickinson & Company
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-02-26
- **Report date:** 2020-05-27
- **Termination date:** 2020-09-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Franklin Lakes, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2075-2020

## Citation

> AI Analytics. FDA recall Z-2075-2020. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/Z-2075-2020. Source: US FDA. Licensed CC0.

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