FDAFDA · Food and drugs·Recall number Z-0423-2026
MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 20 cm;
Published November 12, 2025 · Recall initiated: October 17, 2025
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
A potential issue with the seal integrity of header bag packaging.
What to do
Voluntary: Firm initiated
Recall details
- Manufacturer
- Mozarc Medical US LLC
- Distributor
- US Nationwide distribution.
- Lot
- REF Number: 8888101003HP; UDI-DI: (Individual unit) 10884521127975, (Carton) 20884521127972; Lot number: 2424500194, 2430500018;
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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