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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: FLOWONIX MEDICAL, INC PROMETRA PUMP PROGRAMMER; INFUSION PUMP PROGRAMMER
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FLOWONIX MEDICAL, INC PROMETRA PUMP PROGRAMMER; INFUSION PUMP PROGRAMMER Back to Search Results
Model Number 12828
Medical Device Problem Code Display or Visual Feedback Problem (1184)
Health Effect - Clinical Code No Consequences Or Impact To Patient (2199)
Date of Event 01/26/2016
Type of Reportable Event Malfunction
Additional Manufacturer Narrative
(b)(4).
 
Event or Problem Description
During an initial pump inquiry, the programmer displayed incorrect information.After a few troubleshooting attempts, the programmer appeared to have correctly displayed most of the incorrect information.The device will not be returned for evaluation.
 
Additional Manufacturer Narrative
The manufacture date was corrected in this supplemental report.(b)(4).
 
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Brand Name
PROMETRA PUMP PROGRAMMER
Common Device Name
INFUSION PUMP PROGRAMMER
Manufacturer (Section D)
FLOWONIX MEDICAL, INC
500 international drive
suite 200
mount olive NJ 07828
MDR Report Key5477748
Report Number3006803715-2016-00038
Device Sequence Number325498
Product Code LKK
UDI-Device Identifier00810335020167
UDI-Public010081033502016711150826
Combination Product (Y/N)N
Initial Reporter StateTX
Initial Reporter CountryUS
PMA/510(K) Number
P080012
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source company representative,health
Initial Reporter Occupation Physician
Type of Report Initial,Followup
Report Date (Section B) 02/03/2016
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Operator of Device Physician
Device Model Number12828
Device Catalogue Number12828
Was Device Available for Evaluation? No
Type of Report(Section G)FDA Requested
Initial Date Received by Manufacturer 02/03/2016
Supplement Date Received by ManufacturerNot provided
Initial Report FDA Received Date03/03/2016
Supplement Report FDA Received Date09/08/2016
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)		 No
Patient Sequence Number1
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