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| Catalog Number |
PXSLIMSTR-A |
| Medical Device Problem Code |
Kinked (1339)
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| Health Effect - Clinical Code |
No Consequences Or Impact To Patient (2199)
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| Date of Event |
05/26/2016
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Type of Reportable Event
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Malfunction
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Additional Manufacturer Narrative
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Result: the px slim delivery microcatheter (px slim) was fractured approximately 10.5 cm from the hub and the fractured distal portion was stuck inside a non-penumbra device.The non-penumbra device was ovalized approximately 40.0 cm from the hub.Conclusion: evaluation of the returned devices revealed that the penumbra coil 400 (pc400) sr wire was fractured.This type of damage typically occurs due to improper handling during use.If the device is forcefully withdrawn against resistance, damage such as this may occur.Further evaluation revealed that the pusher assembly was kinked.This type of damage typically occurs due to improper handling during use.If the device is forcefully advanced against resistance, damage such as this may occur.Evaluation of the returned px slim delivery microcatheter (px slim) revealed that the catheter shaft was fractured.This type of damage likely occurs due to improper handling during use.If the device is forcefully manipulated, damage such as this may occur.Further evaluation revealed that the non-penumbra device was ovalized with the fractured distal portion of the px slim stuck inside.The ovalization in the non-penumbra device likely contributed to the resistance that was experienced during advancement and retraction of the pc400.Pc400s are 100% functionally tested during in-process inspection.Px slims are 100% visually inspected during in-process inspection.The manufacturing records for this lot were reviewed and did not reveal any outstanding discrepancies, design, or quality concerns.This report is associated with mfr report number: 3005168196-2016-00890.
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Event or Problem Description
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The patient was undergoing a coil embolization procedure using penumbra coils 400 (pc400) with a px slim delivery microcatheter (px slim).During the procedure, after deploying two loops of a pc400 in the target vessel, the physician noticed the pc400 was unable to advance any further.While attempting to retract the pc400 back into the px slim, the physician experienced resistance; therefore, the pc400 and px slim were removed from the patient.The px slim was reinserted in the patient and after flushing control contrast, the physician noticed the px slim was broken between the hub and the strain relief.The px slim was removed and the procedure was completed using 10 additional pc400 coils with another manufacturermicrocatheter.There was no report of an adverse effect to the patient.
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Search Alerts/Recalls
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