Model Number 20226 |
Device Problems
Device Damaged by Another Device (2915); Device-Device Incompatibility (2919); Material Deformation (2976)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 12/15/2022 |
Event Type
malfunction
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Event Description
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It was reported that stent damage occurred.The target lesion was located in the superficial femoral artery.A 7.0x30x135cm express ld stent was advanced for treatment.However, the device was caught on the sheath and the stent was defective.Subsequently, another 7.0x30x135cm express ld stent was advanced but the device was also caught on the sheath and was also defective.Both devices were retrieved, and the procedure was completed with a different device.There were no patient complications reported and the patient status was stable.
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Manufacturer Narrative
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Device evaluated by mfr: the complaint device was received for analysis.The balloon was received tightly folded which indicates it had not been subjected to positive pressure.The stent was pushed in a distal direction over the distal markerband.No damage or issues were noted with balloon material or stent that could potentially have contributed to the complaint incident.A visual and tactile examination identified no kinks or damage to the shaft of the device.A visual examination of the device identified no issues with the tip that could have contributed to the complaint incident.
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Event Description
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It was reported that stent damage occurred.The target lesion was located in the superficial femoral artery.A 7.0x30x135cm express ld stent was advanced for treatment.However, the device was caught on the sheath and the stent was defective.Subsequently, another 7.0x30x135cm express ld stent was advanced but the device was also caught on the sheath and was also defective.Both devices were retrieved, and the procedure was completed with a different device.There were no patient complications reported and the patient status was stable.
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Search Alerts/Recalls
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