FDA Adverse Event Injury Summary report: N

ONE TOUCH PING GLUCOSE MANAGEMENT SYSTEM

MDR report key: 1790082 · Received August 2, 2010

Report

Report Number
2531779-2010-00836
Event Type
Injury
Date Received
August 2, 2010
Date of Event
July 6, 2010
Report Date
July 6, 2010
Manufacturer
ANIMAS CORP.
Product Code
LZG
PMA / PMN Number
K080639
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE DEVICE HAS BEEN RETURNED TO ANIMAS. EVALUATION HAS NOT YET BEEN COMPLETED. WHEN EVALUATION IS COMPLETE, A SUPPLEMENTAL REPORT WILL BE FILED. IT WAS NOTED THAT THE PATIENT'S INFUSION SITE WAS SCARRED. THE PATIENT CONTACTED ANIMAS AGAIN TO SEEK ADVICE ON HOW TO ROTATE INFUSION SITES. NO CONCLUSIONS CAN BE MADE AT THIS TIME.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT WAS TREATED AT THE EMERGENCY ROOM FOR ELEVATED BLOOD GLUCOSE LEVELS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ONE TOUCH PING GLUCOSE MANAGEMENT SYSTEM INSULIN, INFUSION PUMP LZG ANIMAS CORP. ONE TOUCH PING NA

Patients

Seq Age Sex Outcome Treatment
1 56 YR Hospitalization