FDA Adverse Event Injury Summary report: N

ANIMAS INSULIN INFUSION PUMP

MDR report key: 1153259 · Received September 8, 2008

Report

Report Number
2531779-2008-00545
Event Type
Injury
Date Received
September 8, 2008
Date of Event
July 29, 2008
Report Date
July 29, 2008
Manufacturer
ANIMAS CORP.
Product Code
LZG
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE PUMP WAS RETURNED TO ANIMAS FOR EVALUATION. EVALUATION REVEALED A DAMAGED BUT LEGIBLE DISPLAY SCREEN, BUT DEMONSTRATED THAT INSULIN DELIVERY WAS FUNCTIONING WITHIN REQUIRED SPECIFICATIONS AND DELIVERY ACCURACY.

Description of Event or Problem · 1

THE PATIENT RECEIVED EMERGENCY ROOM TREATMENT FOR 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. IR 1250

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization