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EkoSonic®

EKOS CORPORATION · Model 600-30000 · UDI-DI 00858593006493

KRA Prescription
10
510(k) clearances
9,137
Adverse events (366 deaths)
137
Recalls
150
Facilities

Description

The EkoSonic® Control Unit provides power to the Ultrasonic Core and monitors parameters during operation via the CIC. The Control Unit also provides the user interface for operator control. The EkoSonic® Control Unit is intended exclusively for use with the EkoSonic® Device.

Recalls

DateFirmReason
2026-09-16Boston Scientific Cork, Ltd.The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridge
2026-09-16Boston Scientific Cork, Ltd.The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridge
2026-09-16Boston Scientific Cork, Ltd.The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridge
2026-09-16Boston Scientific Cork, Ltd.The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridge
2026-09-16Boston Scientific Cork, Ltd.The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridge
2026-09-16Boston Scientific Cork, Ltd.The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridge
2026-09-16Boston Scientific Cork, Ltd.The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridge
2026-09-16Boston Scientific Cork, Ltd.The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridge
2026-09-16Boston Scientific Cork, Ltd.The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridge
2026-09-16Boston Scientific Cork, Ltd.The product is defective due to insufficient UV curing of the hydrophilic coating which is present on the outer surface of the distal segment of the microcatheters and raised ridge

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.