Catalog Number C-VH-4001 |
Device Problem
Device Dislodged or Dislocated (2923)
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Patient Problem
No Known Impact Or Consequence To Patient (2692)
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Event Date 04/19/2016 |
Event Type
malfunction
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Manufacturer Narrative
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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.A lot history record review was completed for the reported product lot number.There was no nonconformance recorded in the lot history.(b)(4).
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Event Description
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The hospital reported that during an endoscopic vein harvesting procedure, vasoview hemopro 2 with vasoshield jaws could not be closed due to the electrical prongs being dislodged from the jaws.A replacement device was used to complete the procedure.The hospital did not report any patient effects.The product is returning.
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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 2 with vasoshield jaws could not be closed due to the electrical prongs being dislodged from the jaws.A replacement device was used to complete the procedure.The hospital did not report any patient effects.The product is returning.
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Search Alerts/Recalls
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