# FDA recall Z-3072-2024

> **MEDLINE INDUSTRIES, LP - Northfield** · Class II · device recall initiated 2024-06-18.

## Product

ANESTHESIA TURNOVER KIT, Pack Number DYNJAA0377A

## Reason for recall

A non-sterile Mastisol component, which was not labeled as being sterile or non-sterile, was placed in the non-sterile portion of certain sterile convenience kits and distributed.  In the event that the user assumes sterility during its use, there is an increased risk of patient infection.

## Distribution

US:  TX, IL, CA

## Key facts

- **Recall number:** Z-3072-2024
- **Recalling firm:** MEDLINE INDUSTRIES, LP - Northfield
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-06-18
- **Report date:** 2024-09-18

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3072-2024

## Citation

> AI Analytics. FDA recall Z-3072-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-3072-2024. Source: US FDA. Licensed CC0.

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