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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: SMITHS MEDICAL CADD SOLIS AMBULATORY INFUSION PUMP
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SMITHS MEDICAL CADD SOLIS AMBULATORY INFUSION PUMP Back to Search Results
Model Number 21-2111
Device Problem Device Displays Incorrect Message (2591)
Patient Problem No Consequences Or Impact To Patient (2199)
Event Type  malfunction  
Event Description
A report was received that stated the pump alarmed "error code 44510".No patient injury or adverse event was reported.
 
Manufacturer Narrative
The suspect device was received for evaluation.Testing of the device found error code 44510.Therefore, the circuit board was replaced.Following repair, the device passed all function and delivery testing.
 
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Brand Name
CADD SOLIS AMBULATORY INFUSION PUMP
Manufacturer (Section D)
SMITHS MEDICAL
st. paul MN
Manufacturer (Section G)
SMITHS MEDICAL
1265 grey fox rd.
st. paul MN 55112
Manufacturer Contact
pete hirte
1265 grey fox rd.
st. paul, MN 55112
6516287384
MDR Report Key3786391
MDR Text Key4430831
Report Number2183502-2014-00170
Device Sequence Number1
Product Code MEA
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
K072144
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type User Facility,Company Representative
Reporter Occupation Unknown
Type of Report Initial
Report Date 03/28/2014
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
Device Operator Health Professional
Device Model Number21-2111
Device Catalogue Number21-2111
Was Device Available for Evaluation? Yes
Date Returned to Manufacturer03/18/2014
Is the Reporter a Health Professional? No
Was the Report Sent to FDA? Yes
Date Report Sent to FDA03/28/2014
Device Age2 MO
Event Location Hospital
Initial Date Manufacturer Received 02/28/2014
Initial Date FDA Received03/28/2014
Date Device Manufactured01/01/2014
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Reuse
Patient Sequence Number1
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