| Medical Device Problem Code |
Pumping Problem (3016)
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| Health Effect - Clinical Code |
No Consequences Or Impact To Patient (2199)
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Type of Reportable Event
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Malfunction
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Additional Manufacturer Narrative
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The device has not been returned to animas for evaluation.If the device is returned, an evaluation shall be completed and a supplemental report will be filed.
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Event or Problem Description
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On (b)(6) 2018, a reporter contacted animas alleging that there was an issue with the basal history with their pump.The reporter stated that there were segments where there were 0 units delivered.This complaint is being reported because the alleged issue indicates that there was a delivery problem.There was no allegation of an adverse event associated with this complaint.
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Search Alerts/Recalls
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