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Recall Observatory FDA recall evidence

Device product

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.

Z-2213-2024

May 01, 2024

Class II

Product summary

Firm
Mermaid Medical A/S
Event
Event 94741
Status
Ongoing
Classification
Class II
Quantity
190 devices
Official record key
device-enforcement:Z-2213-2024

Official wording

Reason: Internal product testing failed bubble leak testing (ASTM F2096), which indicates the sterility barrier may not be fully intact.

Code information: Unique Device Identifier: 15711055004333; Lot codes: S2306001; Model Number: T10106065

Distribution pattern: 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.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Internal product testing failed bubble leak testing (ASTM F2096), which indicates the sterility barrier may not be fully intact.