# FDA recall Z-1562-2026

> **Medline Industries, LP** · Class II · device recall initiated 2026-01-30.

## Product

Medline Kits containing Cardinal Health s Aqua-Seal Chest Drainage Unit:  1) OPEN HEART, Model Number: DYNJ902487A;   2) CARDIAC PROCEDURE, Model Number: DYNJ908126;   3) CARDIO CONGENITO, Model Number: DYNJ910851

## Reason for recall

The instructions for use (IFUs) on specified Cardinal Health Chest Drainage Units (CDUs) and accessories have been updated to clarify the intended target patient population as adults, 18 years and older.

## Distribution

Worldwide - US Nationwide distribution in the state of CA and the countries of Chile, Panama.

## Key facts

- **Recall number:** Z-1562-2026
- **Recalling firm:** Medline Industries, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-01-30
- **Report date:** 2026-03-18

- **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-1562-2026

## Citation

> AI Analytics. FDA recall Z-1562-2026. Retrieved 2026-08-17 from https://api.ai-analytics.org/recall/Z-1562-2026. Source: US FDA. Licensed CC0.

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