FDA Adverse Event Malfunction Summary report: N

BELT CLIP

MDR report key: 3981941 · Received August 5, 2014

Report

Report Number
2032227-2014-05273
Event Type
Malfunction
Date Received
August 5, 2014
Date of Event
July 2, 2014
Report Date
July 2, 2014
Manufacturer
MEDTRONIC MINIMED
Product Code
OYC
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI
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 AS NO PRODUCT HAS BEEN RETURNED. NO CONCLUSION CAN BE DRAWN AT THIS TIME. WE, THEREFORE, CONSIDER THIS REPORT COMPLETE TO THE BEST OF OUR KNOWLEDGE.

Description of Event or Problem · 1

IT WAS REPORTED BY THE CUSTOMER THAT THEIR INSULIN PUMP'S BELT CLIP HAD BROKEN. CUSTOMER ALSO STATED THEY WOKE UP IN THE MORNING WITH A BLOOD GLUCOSE LEVEL OF 40 MG/DL DUE TO OVERCORRECTING AFTER EATING A SNACK. CUSTOMER'S BLOOD GLUCOSE LEVEL WAS 92 MG/DL AT TIME OF REPORTING. NOTHING FURTHER REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
457576 BELT CLIP INSULIN INFUSION PUMP / SENSOR AUGMENTED OYC MEDTRONIC MINIMED MMT-642

Patients

Seq Age Sex Outcome Treatment
1 46 YR