FDA Adverse Event Malfunction Summary report: N

PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

MDR report key: 3930488 · Received July 12, 2014

Report

Report Number
2032227-2014-03647
Event Type
Malfunction
Date Received
July 12, 2014
Date of Event
June 2, 2014
Report Date
June 11, 2014
Manufacturer
MEDTRONIC MINIMED
Product Code
OYC
PMA / PMN Number
P980022
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OK
Reporter Occupation
PATIENT

Narratives

Additional Manufacturer Narrative · 1

CURRENTLY, IT IS UNKNOWN WHETHER OR NOT THE DEVICE MAY HAVE CAUSED OR CONTRIBUTED TO THE EVENT. THE DEVICE HAS BEEN RETURNED, BUT NOT YET EVALUATED. FURTHER INFORMATION WILL FOLLOW ONCE THE ANALYSIS HAS BEEN COMPLETED. NO CONCLUSION CAN BE DRAWN AT THIS TIME.

Additional Manufacturer Narrative · 1

THE INSULIN PUMP RECEIVED WITH CRACKED DISPLAY WINDOW CORNERS AND SEVERELY SCRATCHED LCD WINDOW.

Description of Event or Problem · 1

CUSTOMER REPORTED THAT HER BLOOD GLUCOSE WAS 103 MG/DL. CUSTOMER STATED THAT SHE GOT DIZZY AND FELL ON THE INSULIN PUMP. CUSTOMER STATED THAT THE SCREEN IS SCRATCHED AND UNABLE TO READ. NOTHING FURTHER WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
408877 PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP INSULIN INFUSION PUMP / SENSOR AUGMENTED OYC MEDTRONIC MINIMED MMT-723LNAH

Patients

Seq Age Sex Outcome Treatment
1 64 YR