MAUDE Adverse Event Report: STERILMED, INC. REPROCESSED DECANAV EP CATHETER, F CURVE; CATHETER, RECORDING, ELECTRODE, REPROCESSED

Catalog Number	RR7F282CT
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Cardiac Tamponade (2226)
Date of Event	10/13/2025
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
The product analysis lab received the device for evaluation.When the investigational analysis has been completed, a supplemental 3500a report will be submitted.This report is being submitted pursuant to the provisions of 21 cfr, part 803.This report may be based on information which has not been investigated or verified prior to the required reporting date.This report does not reflect a conclusion by sterilmed inc., or its employees that the report constitutes an admission that the product, sterilmed inc., or its employees caused or contributed to the potential event described in this report.If information is obtained that was not available for the initial report, a follow-up report will be filed as appropriate.Manufacturer's ref.No: (b)(4).
Event or Problem Description
It was reported that a patient underwent an atrial fibrillation ablation procedure with a reprocessed decanav ep catheter and the patient experienced a pericardial effusion which required pericardiocentesis.The physician attempted ablation inside the coronary sinus (cs), but due to difficult anatomy it was aborted.The physician attempted both sheath and catheter manipulation inside the cs for approximately 60 minutes.After aborting the ablation, a pericardial effusion was discovered by the post case intracardiac echocardiogram (ice) and confirmed by ice catheter.The physician attempted to perform pericardiocentesis which was aborted due to inability to gain access to the pericardial space, and the physician's impression of the effusion decreasing.The patient¿s condition worsened and the patient began showing tamponade physiology later in the day and was brought back to the lab for pericardiocentesis which was successful in removing 300ml of fluid.The patient was stable.Last known status of the patient is improved.The patient required extended hospitalization because of continued monitoring.One transseptal puncture was performed with baylis nrg.Prior to noting the pericardial effusion, ablation was performed.The patient did not require cardiac surgery.No evidence of steam pop.The procedural activated clotting time was 350 seconds.The flow setting was standard settings.The correct catheter settings were selected on the generator.No issues with flow rate change at the start of ablation.No error messages observed on biosense webster equipment during the procedure.The visitag module parameters for stability used were 2mm, 3 seconds and 25% of 3g.No additional filter was used with the visitag.The color option prospectively used was tag index.The physician¿s opinion on the cause of this adverse event was difficult patient anatomy along with manipulation of catheters and sheaths inside the cs.The smarttouch surround flow catheter, decanav catheter, vizigo sheath, and sl1 sheath were all used in attempting to access the cs.However, it is unclear which specific device led to the effusion.
Additional Manufacturer Narrative
It was reported that a patient underwent an atrial fibrillation ablation procedure with a reprocessed decanav ep catheter and the patient experienced a pericardial effusion which required pericardiocentesis.The device was returned to sterilmed for further evaluation.A non-sterile reprocessed decanav ep catheter was received contained in the decontamination bag.Upon receiving the device, visual inspection was performed, and the serial number label was missing from the shaft of the catheter.No appearance of damage was noted.Physical mark on the device indicated it had been reprocessed (1) time.The catheter was connected to the carto 3 system, and it was recognized and visualized without anomalies.A device history record (dhr) was performed, and no internal actions were identified.No further investigation is being conducted as there is no alleged quality issue against the reprocessed catheter.This investigation is considered complete at this time; if additional information is received at a later time, this investigation will be updated, and further actions can be taken as needed.As part of sterilmed's quality process all devices are manufactured, inspected, and released to approved specifications.There was no evidence to suggest the event was related to a manufacturing or design issue.If additional information is received regarding this event, a supplemental 3500a report will be submitted to the fda.Manufacturer's ref.No: (b)(4).

• Brand Name: REPROCESSED DECANAV EP CATHETER, F CURVE
• Common Device Name: CATHETER, RECORDING, ELECTRODE, REPROCESSED
• Manufacturer (Section D): STERILMED, INC.; 5010 cheshire parkway; ste 2; plymouth MN 55446
• Manufacturer (Section G): STERILMED, INC.; 5010 cheshire parkway; ste 2; plymouth MN 55446
• Manufacturer Contact: henry boden ; 31 technology dr; irvine, CA 92618 ; 9497882078
• MDR Report Key: 23459236
• Report Number: 2134070-2025-00031
• Device Sequence Number: 8345142
• Product Code: NLH
• UDI-Device Identifier: 10888551045704
• UDI-Public: (01)10888551045704(17)270410(10)2235232
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K240826
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional,Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Catalogue Number: RR7F282CT
• Device Lot Number: 2235232
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 10/30/2025
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 10/13/2025
• Supplement Date Received by Manufacturer: 11/07/2025
• Initial Report FDA Received Date: 11/03/2025
• Supplement Report FDA Received Date: 12/01/2025
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 04/10/2025
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): Yes
• Usage of Device: Initial
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: 8.5F SHEATH WITH CURVE VIZ MDC; BAYLIS NRG; CARTO 3 SYSTEM; NGEN PUMP; NGEN¿ GENERATOR; SOUNDSTAR ECO 8F DIAGNOSTIC ULTRASOUND CATHETER; THMCL SMTCH SF BID, TC, D-F
• Outcome Attributed to Adverse Event: Required Intervention; Hospitalization; Life Threatening
• Patient Sex: Male
• Patient Ethnicity: Non Hispanic
• Patient Race: White