# FDA recall Z-2378-2018

> **Medline Industries, Inc.** · Class II · device recall initiated 2018-01-12.

## Product

BARD MYPICC Kit, REF CK000095B, 5F French Size, packaged 5 kits/case, Sterile, RX, For use in vascular access procedures.

## Reason for recall

One of the cases of product might not have been sterilized.

## Distribution

The product was distributed to UT.

## Key facts

- **Recall number:** Z-2378-2018
- **Recalling firm:** Medline Industries, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-01-12
- **Report date:** 2018-07-18
- **Termination date:** 2020-07-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Waukegan, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2378-2018

## Citation

> AI Analytics. FDA recall Z-2378-2018. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-2378-2018. Source: US FDA. Licensed CC0.

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