Recall Z-0133-2014

EKOS Corporation · initiated October 2, 2013

Class II Terminated

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

The EkoSonic Endovascular System employs high frequency (2-2.5 MHz), low power (0.585 watt average power per transducer) ultrasound to facilitate the delivery of physician-specified fluids in the peripheral vasculature and to deliver solutions into the pulmonary arteries. The EkoSonic Endovascular System is intended for the controlled and selective infusion of physician-specified fluids, including thrombolytics, into the peripheral vasculature and the infusion of solutions into the pulmonary arteries. The reusable EKOS EkoSonic Control Unit provides power to the system and the user interface for operator control. A reusable, non sterile Connector Interface Cable connects the EKOS EkoSonic Control Unit to the EkoSonic Endovascular Device.

Codes / lots: PT3B-783. PT3B represents the model number. Adding 783 creates the serial number.

Reason for recall

The EkoSonic Control Unit is recalled because it had the incorrect power entry module installed. It is missing an AC filter to reduce the noise and electrical interference.

FDA-determined cause: Mixed-up of materials/components

Action taken

EKOS notified their customer by email on October 2, 2013, about the recall. EKOS has requested the customer to return of EkoSonic Control Unit PT3B-783, so that it can be replaced. CORRECTIVE ACTION: This single affected unit will be reworked with the correct power entry module and released into finished goods as a refurbished control unit. EKOS did not distributed any affected devices in the US. For any questions, please call EKOS Corporation at 425-415-3100.

Details

Recall number
Z-0133-2014
Initiated
October 2, 2013
Posted by FDA
November 1, 2013
Terminated
November 22, 2013
Product code
KRA – Catheter, Continuous Flush
Quantity
one unit
Distribution
Worldwide Distribution in Germany only.
Recalling firm
EKOS Corporation, Bothell, WA

Official FDA recall record