FDA Adverse Event Injury Summary report: N

BELT CLIP PUMP CLEAR

MDR report key: 4233449 · Received November 6, 2014

Report

Report Number
2032227-2014-48864
Event Type
Injury
Date Received
November 6, 2014
Date of Event
September 1, 2014
Report Date
October 9, 2014
Manufacturer
MEDTRONIC MINIMED
Product Code
OYC
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
NY
Reporter Occupation
OTHER

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 THE CUSTOMER WAS IN THE EMERGENCY ROOM FOR A MENTAL BREAKDOWN. THE CUSTOMER ALSO STATED SHE WAS UNABLE TO LOCATE HER BELT CLIP. NO ADDITIONAL INFORMATION PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
712752 BELT CLIP PUMP CLEAR INSULIN INFUSION PUMP / SENSOR AUGMENTED OYC MEDTRONIC MINIMED MMT-631CL

Patients

Seq Age Sex Outcome Treatment
1 51 YR Hospitalization