Model Number VASOVIEW HEMOPRO 2 |
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 06/20/2019 |
Event Type
malfunction
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Manufacturer Narrative
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Trackwise id : (b)(4).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.Device not returned.
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Event Description
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The hospital reported that during an endoscopic vein harvesting procedure using vasoview hemopro 2, no c02 flowed through the system.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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Internal complaint number: 222138.Device evaluated by mfr: the device was discarded.
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Event Description
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The hospital reported that during an endoscopic vein harvesting procedure using vasoview hemopro 2, no c02 flowed through the system.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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