FDA Adverse Event Malfunction Summary report: N

ANIMAS INSULIN INFUSION PUMP

MDR report key: 1163310 · Received September 9, 2008

Report

Report Number
2531779-2008-00565
Event Type
Malfunction
Date Received
September 9, 2008
Date of Event
August 7, 2008
Report Date
August 7, 2008
Manufacturer
ANIMAS CORP.
Product Code
LZG
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CT, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE PUMP WAS RETURNED TO ANIMAS FOR EVALUATION. EVALUATION REVEALED AN INTERMITTENT LOSS OF CONTACT BETWEEN THE BATTERY CAP AND THE PUMP CASE.

Description of Event or Problem · 1

THE PATIENT REPORTED THAT THE PUMP WAS RESETTING ITSELF WITHOUT INTERVENTION. THE PATIENT ALSO EXPERIENCED ELEVATED BLOOD GLUCOSE LEVELS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ANIMAS INSULIN INFUSION PUMP INSULIN INFUSION PUMP LZG ANIMAS CORP. ANIMAS 2020

Patients

Seq Age Sex Outcome Treatment
1 67 YR