Catalog Number CON-HL-90 |
Device Problem
Power Problem (3010)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Type
malfunction
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Manufacturer Narrative
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The device was unable to be evaluated as it was not returned.If the device is received in the future an evaluation will be performed.The reported event was unable to be confirmed or replicated.A cause of the reported event could not be determined at this time.
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Event Description
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It was reported that the fluid warming device had a power switch problem.No patient injury reported.
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Manufacturer Narrative
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Other text: manufacturing device history record review was not performed because the results of the complaint investigation do not indicate a problem with the manufacture of the device.No causes or potential causes of the customer's reported problem were found during the review of service and repair records.E4 and udi section of d4 are unknown, no product information has been provided to date.
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Search Alerts/Recalls
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