FDAFDA · Food and drugs·Recall number Z-2213-2024
The D*Clot¿ HD Rotational Thrombectomy System is a percutaneous catheter-based system available in 6 French. The disposable system consists of an outer sheath through which a rotatable radiopaque spiral shaft extends ending in an eccentric blunt distal tip. Once activated, the shaft rotates at approximately 10.000 RPMs to break thrombus into smaller particles, which can be simultaneously aspirated using a dedicated vacuum syringe. The catheter is a stand-alone system and is powered by a 4.5 VDC alkaline battery pack in the control unit.
Published July 3, 2024 · Recall initiated: May 1, 2024
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
Internal product testing failed bubble leak testing (ASTM F2096), which indicates the sterility barrier may not be fully intact.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- Mermaid Medical A/S
- Distributor
- Worldwide - US Nationwide distribution in the states of OH, MO, CO, NC, TX, MA, GA, FL, IL, IN, MD, PA, VA, and the country of Chile.
- Lot
- Unique Device Identifier: 15711055004333; Lot codes: S2306001; Model Number: T10106065
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- Denmark
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