D*Clot HD Thrombectomy System (Mermaid Medical) – Bubble Leak (2024)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
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
Brand
Mermaid Medical A/S Frydensbergvej 25 Stenlose Denmark
Lot Codes / Batch Numbers
Unique Device Identifier: 15711055004333, Lot codes: S2306001, Model Number: T10106065
Products Sold
Unique Device Identifier: 15711055004333; Lot codes: S2306001; Model Number: T10106065
Mermaid Medical A/S Frydensbergvej 25 Stenlose Denmark is recalling The D*Clot HD Rotational Thrombectomy System is a percutaneous catheter-based system available in 6 due to Internal product testing failed bubble leak testing (ASTM F2096), which indicates the sterility barrier may not be fully intact.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Internal product testing failed bubble leak testing (ASTM F2096), which indicates the sterility barrier may not be fully intact.
Recommended Action
Per FDA guidance
The consignees and distributors were sent out the notification via email on 05/01/2024. The letter instructs the consignees to: 1. Quarantine and Discontinue Use of Affected Product: Identify, segregate, and discontinue use of the affected product in your inventory. 2. Complete and Return the attached Response Form: Complete the attached Response Form and return to Mermaid Medical by May 10, 2024 via email or by post. 3. Distributors/ If You Further Distributed Affected Product: Forward this communication to any customers that were distributed affected product. Instruct any of your customers to complete the response form and return to Mermaid Medical. Once they complete and return the response form, Mermaid Medical will provide instructions on how to return or destroy any affected product remaining in their inventory.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026