Model Number H749RB4250100 |
Device Problem
Material Rupture (1546)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 12/07/2016 |
Event Type
malfunction
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Manufacturer Narrative
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Age at the time of event: 18 years or older.(b)(4).
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Event Description
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It was reported that a balloon rupture occurred.The 90% stenosed target lesion was located in the moderately tortuous and severely calcified left anterior descending (lad) artery.A 10/2.50 flextome cutting balloon was selected for use.During the procedure, while on continuous flushing, it was noted that the pressure would not rise as the balloon ruptured.The device was removed from the patient's body and completed the procedure with another of the same device.There were no patient complications reported.
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Manufacturer Narrative
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Device evaluated by mfr: the device was returned for analysis.A visual examination identified that the balloon was not folded which indicates that the balloon was subjected to positive pressure.Blood was identified within the balloon and inflation lumen which is evidence of a device leak.The returned device was attached to an encore inflation unit.Positive pressure was applied when liquid was observed to be leaking from a balloon pinhole at 2.0mm distal to the distal end of the proximal marker band.An examination of the balloon material and markerbands identified no issues which could potentially have contributed to this complaint.A visual and microscopic examination observed no damage to the tip or blades.All blades were present and fully bonded to the balloon surface.The hypotube was kinked at several locations along its length.No other issues were identified during the product analysis.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).
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Event Description
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It was reported that a balloon rupture occurred.The 90% stenosed target lesion was located in the moderately tortuous and severely calcified left anterior descending (lad) artery.A 10/2.50 flextome¿ cutting balloon¿ was selected for use.During the procedure, while on continuous flushing, it was noted that the pressure would not rise as the balloon ruptured.The device was removed from the patient's body and completed the procedure with another of the same device.There were no patient complications reported.
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Search Alerts/Recalls
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