Model Number VASOVIEWHEMPRO (US) VH-3000 |
Device Problem
Improper Flow or Infusion (2954)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 02/14/2020 |
Event Type
malfunction
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Manufacturer Narrative
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Trackwise id #293802.A lot history record review was completed for the reported product lot number.There were no ncmr¿s for the reported lot number.The device has not yet been returned to maquet cardiac surgery for evaluation.We are following up with the customer for the return of the device.A supplemental report will be submitted if the device is received.
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Event Description
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The hospital reported that during an endoscopic vein harvesting procedure, vasoview hemopro saline flush port would not allow saline to flow through to the distal end of the hemopro.Several attempts were made but with no success.A replacement device was used to complete the procedure.The hospital did not report any patient effects.
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Manufacturer Narrative
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(b)(4).
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Event Description
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The hospital reported that during an endoscopic vein harvesting procedure, vasoview hemopro saline flush port would not allow saline to flow through to the distal end of the hemopro.Several attempts were made but with no success.A replacement device was used to complete the procedure.The hospital did not report any patient effects.
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Search Alerts/Recalls
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