FDA Adverse Event Malfunction Summary report: N

RSVR MMT-326A 10PK PRDGM 1.8ML 13L

MDR report key: 1031919 · Received April 16, 2008

Report

Report Number
2032227-2008-00646
Event Type
Malfunction
Date Received
April 16, 2008
Date of Event
April 1, 2008
Report Date
April 1, 2008
Manufacturer
MEDTRONIC MINIMED
Product Code
FMF
PMA / PMN Number
K001828
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MD, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

CURRENTLY, IT IS UNK WHETHER OR NOT THE DEVICE MAY HAVE CAUSED OR CONTRIBUTED TO THE EVENT AS NO PRODUCT HAS BEEN RETURNED. WE THEREFORE CONSIDER THIS REPORT COMPLETE TO THE BEST OF OUR KNOWLEDGE. NO CONCLUSION CAN BE DRAWN AT THIS TIME.

Description of Event or Problem · 1

THE CUSTOMER STATED THAT INSULIN LEAKED FROM THE RESERVOIR AT THE O-RINGS. NOTHING FURTHER WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 RSVR MMT-326A 10PK PRDGM 1.8ML 13L DISPOSABLES FMF MEDTRONIC MINIMED MMT-326A

Patients

Seq Age Sex Outcome Treatment
1