Model Number 21-7302-24 |
Device Problem
Excess Flow or Over-Infusion (1311)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Type
malfunction
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Event Description
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It was reported that after changing the cassette, the patient felt that they were receiving too much medication.The position of the pump when the event occurred is unknown.The reported product fault occurred while in use with the patient.The product issue did not cause or contributed to patient or clinical injury.
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Manufacturer Narrative
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Operator of device is unknown.No information has been provided to date.
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Manufacturer Narrative
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No problems or issues were identified during this device history record (dhr) review.No product was returned; therefore, the reported complaint could not be confirmed and the root cause could not be determined.If the product is returned, this complaint will be reopened for further investigation.
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Search Alerts/Recalls
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