Model Number INFKIT2 |
Device Problem
Insufficient Flow or Under Infusion (2182)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 05/03/2021 |
Event Type
malfunction
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Manufacturer Narrative
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The pump was not returned to mmdg for evaluation.A dhr review was completed and no non conformances were found.Because the pump was not returned to mmdg, no investigation could be completed.This report will be updated if the pump is returned to mmdg.
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Event Description
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The initial reporter stated that the pump was under infusing.They stated that the feeding was programmed for an hour, but that it took an hour and a half to deliver.The initial reporter did not report any adverse effect to the patient, but also declined to provide any additional information.(b)(4).
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Event Description
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The initial reporter stated that the pump was under infusing.They stated that the feeding was programmed for an hour, but that it took an hour and a half to deliver.The initial reporter did not report any adverse effect to the patient, but also declined to provide any additional information.[complaint (b)(4)].
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Manufacturer Narrative
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The pump was returned to mmdg for evaluation.A dhr review was completed and no non-conformances were found.When the device was returned to mmdg, it operated as expected.Mmdg could not replicate or confirm the reported complaint.Based on this information, no mdr would have been required.
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Search Alerts/Recalls
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