FDA Adverse Event Malfunction Summary report: N

RSVR MMT-332A 10PK PRDGM 3CC 14L

MDR report key: 1874020 · Received October 15, 2010

Report

Report Number
2032227-2010-82926
Event Type
Malfunction
Date Received
October 15, 2010
Date of Event
September 25, 2010
Report Date
September 25, 2010
Manufacturer
MEDTRONIC MINIMED
Product Code
FMF
PMA / PMN Number
K032005
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NC, US
Reporter Occupation
NOT APPLICABLE

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. THE DEVICE WILL BE RETURNED FOR ANALYSIS AND FURTHER INFORMATION WILL FOLLOW ONCE THE ANALYSIS HAS BEEN COMPLETED. NO CONCLUSION CAN BE DRAWN AT THIS TIME.

Description of Event or Problem · 1

THE CUSTOMER'S MOTHER REPORTED THAT INSULIN LEAKED PAST THE O-RINGS AND INTO THE RESERVOIR COMPARTMENT. NOTHING FURTHER WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 RSVR MMT-332A 10PK PRDGM 3CC 14L RESERVOIR FMF MEDTRONIC MINIMED MMT-332A GG0606543

Patients

Seq Age Sex Outcome Treatment
1 18 YR