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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: BD / CAREFUSION PYXIS ES

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BD / CAREFUSION PYXIS ES Back to Search Results
Device Problems Data Problem (3196); Patient Data Problem (3197); Application Program Problem: Medication Error (3198)
Patient Problem No Information (3190)
Event Type  Other  
Event Description
I wanted to report a suboptimal design issue with pyxis es that has contributed to errors at our hospital.Unload/load transactions when a new medication is pend loaded on top of a medication to be unloaded, pyxis automatically schedules the transactions so that the unload transaction is immediately followed by the subsequent load (while pocket is still open from unload transaction).There is no way to perform all unload transactions, then go back and do the load transactions.This workflow is quicker (touch each pocket once).However, we have had numerous cases where the tech forgets to remove the medication to be unloaded before putting the new medication into the pocket.Medication administered to or used by the pt: no.(b)(4).Ref: mw5066024.
 
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Brand Name
PYXIS ES
Type of Device
PYXIS ES
Manufacturer (Section D)
BD / CAREFUSION
MDR Report Key6102228
MDR Text Key60078876
Report NumberMW5066025
Device Sequence Number1
Product Code NZH
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Type of Report Initial
Report Date 08/19/2016
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received11/11/2016
Is this an Adverse Event Report? No
Is this a Product Problem Report? No
Device Operator No Information
Type of Device Usage N
Patient Sequence Number1
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