Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1562-2026 — 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

U.S. FDA — Device Enforcement · United States · 2026-01-30 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1562-2026
Date of alert
2026-01-30
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Medline Industries, LP
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10193489496635
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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