Model Number 8002-062-626 |
Device Problem
Fluid/Blood Leak (1250)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 10/01/2020 |
Event Type
malfunction
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Manufacturer Narrative
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This record is a consolidation of records summarized as part of the fda voluntary malfunction summary reporting program. 1 device is pending investigation. there was no remedial action taken. this device is not labeled for single use.
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Event Description
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This report summarizes 1 malfunction event, where it was reported fluid leaks onto patient support surface area. there was no patient involvement.
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Event Description
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This report summarizes 1 malfunction event, where it was reported fluid leaks onto patient support surface area. there was no patient involvement.
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Manufacturer Narrative
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The device that was pending evaluation was not made available by the customer; the reported issue was not confirmed.
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Search Alerts/Recalls
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