MAUDE Adverse Event Report: ST. JUDE MEDICAL INQUIRY AFOCUS LL DIAGNOSTIC CATHETER; CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING

Model Number	IBI-81594
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Cardiac Perforation (2513)
Date of Event	09/18/2020
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
The results of the investigation are inconclusive since the device was not returned for analysis.The device history record was reviewed to ensure that each manufacturing and inspection operation was performed.Based on the information received, the cause of the reported incident could not be conclusively determined.Per the ifu, cardiac perforation is a known risk during the use of this device.
Event or Problem Description
Related manufacturer report numbers: 3005334138-2020-00465, 2182269-2020-00087, 3005334138-2020-00466, 3008452825-2020-00521.At the end of a pvc ablation procedure, during rf of the last lesion, a pericardial effusion occurred.The duo catheter was placed in the coronary sinus and the flexability was used for ablation of the pvc's in the right ventricle.Reinforcement of the lesions in the right ventricle were verified to confirm elimination of the arrhythmia.However, the patient became hypotensive and an echocardiogram revealed a pericardial effusion.A pericardiocentesis was performed to stabilize the patient.There were no performance issues with any abbott devices.

• Brand Name: INQUIRY AFOCUS LL DIAGNOSTIC CATHETER
• Common Device Name: CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING
• Manufacturer (Section D): ST. JUDE MEDICAL; 2375 morse ave; irvine CA 92614
• MDR Report Key: 10669306
• Report Number: 2030404-2020-00083
• Device Sequence Number: 2880883
• Product Code: DRF
• UDI-Device Identifier: 05414734305006
• UDI-Public: 05414734305006
• Combination Product (Y/N): N
• Initial Reporter Country: BR
• PMA/510(K) Number: K010471
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Physician
• Type of Report: Initial
• Report Date (Section B): 10/13/2020

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 Expiration Date: 03/31/2022
• Device Model Number: IBI-81594
• Device Catalogue Number: IBI-81594
• Device Lot Number: 6947171
• Was Device Available for Evaluation?: No
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 09/18/2020
• Initial Report FDA Received Date: 10/13/2020
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: BRK NEEDLE; FLEXABILITY CATHETER; LIVEWIRE CATHETER; SWARTZ BRAIDED
• Outcome Attributed to Adverse Event: Required Intervention