| Model Number |
10603 |
| Medical Device Problem Code |
Break (1069)
|
| Health Effect - Clinical Code |
No Consequences Or Impact To Patient (2199)
|
| Date of Event |
05/09/2019
|
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Type of Reportable Event
|
Malfunction
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Additional Manufacturer Narrative
|
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Device is a combination product.
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| |
|
Event or Problem Description
|
|
It was reported that shaft break occurred.The target lesion was located in left circumflex.A 2.50x20mm synergy stent was advanced to treat the lesion.However, the device failed to cross the lesion and the shaft got broken.No patient complications were reported.
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Search Alerts/Recalls
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