UNK_NAVISTAR THERMOCOOL
Report
- Report Number
- 2029046-2020-00794
- Event Type
- Injury
- Date Received
- June 30, 2020
- Date of Event
- January 1, 2018
- Report Date
- June 10, 2020
- Manufacturer
- BIOSENSE WEBSTER INC
- Product Code
- LPB
- PMA / PMN Number
- UNK
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Occupation
- PHYSICIAN
Narratives
PRODUCT COMPLAINT # (B)(4). SINCE THE PRODUCT WAS NOT RETURNED FOR ANALYSIS, NO PRODUCT FAILURE ANALYSIS CAN BE CONDUCTED AND NO DETERMINATION OF POSSIBLE CONTRIBUTING FACTORS COULD BE MADE. DEVICE HISTORY RECORD (DHR) REVIEW CANNOT BE CONDUCTED BECAUSE NO LOT NUMBER WAS PROVIDED BY THE CUSTOMER. INFORMATION REGARDING PATIENT WEIGHT, HEIGHT, MEDICAL HISTORY, RACE, AND ETHNICITY WAS NOT REPORTED. BIOSENSE WEBSTER MANUFACTURER'S REPORT NUMBER 2029046-2020-00795 IS RELATED TO THE SAME INCIDENT.
THIS COMPLAINT IS FROM A LITERATURE SOURCE. AS REPORTED IN THE LITERATURE PUBLICATION ENTITLED ¿EFFICACY OF HYBRID THERAPY USING PRIOR ADMINISTRATION OF BEPRIDIL HYDROCHLORIDE AND CRYOBALLOON ABLATION IN PATIENTS WITH PERSISTENT ATRIAL FIBRILLATION¿ 1 PATIENT WITH PERSISTENT ATRIAL FIBRILLATION WHO UNDERWENT ATRIAL FIBRILLATION CATHETER ABLATION FROM NON-RECURRENCE GROUP EXPERIENCED CARDIAC TAMPONADE. PURPOSE OF THIS STUDY TO INVESTIGATE THE EFFICACY OF PRETREATMENT WITH BEPRIDIL PRIOR TO CRYOBALLOON ABLATION (CBA) WITH RESPECT TO CLINICAL OUTCOMES IN PATIENTS WITH PERSISTENT ATRIAL FIBRILLATION. METHODS: FROM NOVEMBER 2015 TO APRIL 2018 65 CONSECUTIVE PATIENTS WITH PEAF WHO UNDERWENT CBA FOLLOWING PRETREATMENT WITH BEPRIDIL HYDROCHLORIDE (BEPRIDIL). ELECTRICAL CARDIOVERSION WAS ADDITIONALLY PERFORMED IN CASES INVOLVING THE FAILURE OF PHARMACOLOGICAL SINUS RESTORATION BEFORE CBA. THE PRIMARY ENDPOINT WAS SURVIVAL FREE FROM ATRIAL TACHYARRHYTHMIA AT THE ONE-YEAR FOLLOW-UP, AND THE SECONDARY ENDPOINTS WERE CHANGES IN P-WAVE MORPHOLOGY AND LEFT ATRIUM DIAMETER (LAD) BEFORE CRYOBALLOON ABLATION WERE RETROSPECTIVELY ANALYZED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 679922 | UNK_NAVISTAR THERMOCOOL | CARDIAC ABLATION PERCUTANEOUS CATHETER | LPB | BIOSENSE WEBSTER INC |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 64 YR | Other |