{ "meta": { "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.", "terms": "https://open.fda.gov/terms/", "license": "https://open.fda.gov/license/", "last_updated": "2026-08-20", "results": { "skip": 0, "limit": 1, "total": 1 } }, "results": [ { "cfres_id": "41817", "product_res_number": "Z-0175-06", "event_date_initiated": "2005-01-18", "event_date_posted": "2005-11-23", "recall_status": "Terminated", "event_date_terminated": "2005-11-29", "res_event_number": "33408", "product_code": "KRA", "k_numbers": [ "K042456" ], "product_description": "Lysus Infusion System - PT-3 Control . The Lysus Infusion System employs high frequency (2-2.5 MHz), low power (0.45 watt average power per transducer) ultrasound to facilitate the delivery of physician-specified fluids in the peripheral vasculature. (This system is also called the UltraFlo and EKOS Peripheral Infusion System in internal documents.)\n\nThe Lysus Infusion System consists of three main components, a single use Lysus Infusion Catheter System which is comprised of a Drug Delivery Catheter (DDC) and removable Ultrasound Core (USC), and a reusable EKOS PT-3 Control System. During use, fluids are delivered through the side-holes of the DDC. The USC is placed through the central lumen of the DDC to deliver ultrasound energy along the length of fluid delivery, dispersing the fluid into the intravascular treatment site. The reusable EKOS PT-3 Control Unit provides power to the system and the user interface for operator control. A reusable, non-sterile Catheter Interface Cable with Pod connects the EKOS PT-3 Control Unit to the Lysus Infusion Catheter System.", "code_info": "Serial numbers PT3-002, PT3-006, PT3-007, PT3-009, PT3-012, PT3-013, PT3-014", "firm_fei_number": "3001627457", "recalling_firm": "Ekos Corp", "address_1": "22030 - 20th Ave SE, Ste 101 22030 20th Ave SE", "address_2": "Ste 101", "city": "Bothell", "state": "WA", "postal_code": "98021", "additional_info_contact": "Jocelyn Kersten\n425-482-1108 Ext. 287", "reason_for_recall": "Potential for a faulty thermal channel offset to be reported to the software causing faulty lower temperature values to be reported which allow a power increase.", "root_cause_description": "Other", "action": "On 1/19/05 the firm began visiting consignees and upgrading software.", "product_quantity": "7", "distribution_pattern": "The device was distributed to 6 hospitals/medical centers; 1 each located in AZ, OH, WA, FL, IL, and. CA. One consignee is located Germany.", "openfda": { "k_number": [ "K010004", "K153502", "K082519", "K111490", "K101450", "K964868", "K971306", "K931335", "K993266", "K953133", "K070279", "K040139", "K230636", "K172081", "K214025", "K082613", "K072724", "K180275", "K210114", "K952874", "K951602", "K231279", "K023351", "K003925", "K951502", "K070979", "K801173", "K100892", "K161962", "K860570", "K211525", "K153501", "K132947", "K924661", "K223176", "K885281", "K062752", "K093750", "K142259", "K113773", "K111263", "K034036", "K954020", "K832058", "K914751", "K780479", "K123477", "K161921", "K923368", "K033913", "K042187", "K250794", "K000177", "K052738", "K212719", "K030688", "K231148", "K874242", "K060224", "K243534", "K202318", "K955525", "K161801", "K131772", "K152625", "K050205", "K071468", "K210339", "K163701", "K160884", "K223139", "K962129", "K020680", "K171665", "K980104", "K070384", "K182071", "K213442", "K201792", "K884946", "K761273", "K965189", "K181684", "K080737", "K945909", 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"device_name": "Catheter, Continuous Flush", "medical_specialty_description": "Cardiovascular", "regulation_number": "870.1210", "device_class": "2" } } ] }