MAUDE Adverse Event Report: BOSTON SCIENTIFIC - COSTA RICA (HEREDIA) BLAZER® II XP; CATHETER, PERCUTANEOUS, CARDIAC ABLATION, FOR TREATMENT OF ATRIAL FLUTTER

Model Number	M0044790THK20
Medical Device Problem Codes	Charred (1086); Device Operates Differently Than Expected (2913)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	11/21/2016
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
(b)(4).Device evaluated by mfr: the device has not been received for analysis.Upon receipt and completion of the failure analysis of the complaint device, if there is any further relevant information from that review, a supplemental medwatch will be filed.(b)(4).
Event or Problem Description
Same case as mdr id 2134265-2016-11315.It was reported that there was char on the device, and steam pops occurred.The target lesion was located in the cavotricuspid isthmus(cti).A blazer® ii xp was selected for use.On the middle of a flutter ablation, it was noted that the first two catheter used seemed to be not ablating sufficiently and properly.In addition, steam pops were heard and the expected reduction in electrogram amplitude during successful tissue ablation was not observed.The catheter was then removed from the patient's body; however, a char on the proximal edge of the distal electrodes were noted.The procedure was completed with another of the same device.No patient complications reported and patient's condition was fine.
Additional Manufacturer Narrative
Updated: device avail.For eval, returned to mfr.On, device returned to mfr., device evaluated by mfr., eval summary attached, method codes, result codes, conclusion codes device evaluated by manufacturer: the device was returned for analysis.Unit was received for analysis after decontamination (in appropriate packaging).Visual inspection revealed that there is dried body fluid and char present on the proximal end of the distal tip.No char is present on the rings.Electrical test was performed by using the multimeter and the device was found within specifications.No opens or shorts were found.The ablation was verified by using the maestro generator 4000 and the device was found within specifications.The manufacturing batch record review confirmed that the device met all material, assembly and performance specifications.The most probable root cause is operational context as device performance was limited due to anatomical/procedural factors.(b)(4).
Event or Problem Description
Same case as mdr id 2134265-2016-11315.It was reported that there was char on the device, and steam pops occurred.The target lesion was located in the cavotricuspid isthmus(cti).A blazer® ii xp was selected for use.On the middle of a flutter ablation, it was noted that the first two catheter used seemed to be not ablating sufficiently and properly.In addition, steam pops were heard and the expected reduction in electrogram amplitude during successful tissue ablation was not observed.The catheter was then removed from the patient's body; however, a char on the proximal edge of the distal electrodes were noted.The procedure was completed with another of the same device.No patient complications reported and patient's condition was fine.

• Brand Name: BLAZER® II XP
• Common Device Name: CATHETER, PERCUTANEOUS, CARDIAC ABLATION, FOR TREATMENT OF ATRIAL FLUTTER
• Manufacturer (Section D): BOSTON SCIENTIFIC - COSTA RICA (HEREDIA); 302 parkway; la aurora; heredia ; CS
• MDR Report Key: 6190804
• Report Number: 2134265-2016-11316
• Device Sequence Number: 18845203
• Product Code: OAD
• UDI-Device Identifier: 08714729452386
• UDI-Public: (01)08714729452386(17)20190802(10)0019532253
• Combination Product (Y/N): N
• Initial Reporter State: HI
• Initial Reporter Country: US
• PMA/510(K) Number: P020025
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 11/21/2016

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Expiration Date: 08/02/2019
• Device Model Number: M0044790THK20
• Device Catalogue Number: 4790THK2
• Device Lot Number: 0019532253
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 03/22/2017
• Type of Report(Section G): FDA Requested
• Initial Date Received by Manufacturer: 11/21/2016
• Supplement Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 12/20/2016
• Supplement Report FDA Received Date: 04/21/2017
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1