FDA Adverse Event Malfunction Summary report: N

ANIMAS INSULIN CARTRIDGE

MDR report key: 2042895 · Received March 30, 2011

Report

Report Number
2531779-2011-02088
Event Type
Malfunction
Date Received
March 30, 2011
Report Date
February 28, 2011
Manufacturer
ANIMAS CORP.
Product Code
LZG
PMA / PMN Number
K032257
Removal / Correction Number
2531779-02/25/11-001-R
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TN, US
Reporter Occupation
UNKNOWN

Narratives

Additional Manufacturer Narrative · 1

THE CARTRIDGE WAS NOT RETURNED TO ANIMAS. ALTHOUGH THE CARTRIDGE WAS NOT RETURNED THERE IS NO FURTHER INVESTIGATION NECESSARY WITH RESPECT TO THE LEAK ISSUE. CARTRIDGES WITH LOT # B201581 WERE CONFIRMED TO BE DEFECTIVE. WHEN TESTED, FLUID WAS OBSERVED LEAKING FROM THE PLUNGER END OF THE CARTRIDGE.

Description of Event or Problem · 1

IT WAS REPORTED THAT IN LATE DECEMBER, THE PATIENT HAD ONE LEAKING CARTRIDGE WHERE THE PLUNGER MEETS THE BARREL OF THE CARTRIDGE. SHE REPORTED NO BLOOD GLUCOSE EXCURSIONS. THE PATIENT IS ABLE TO USE THE PUMP.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ANIMAS INSULIN CARTRIDGE INSULIN INFUSION PUMP CARTRIDGE LZG ANIMAS CORP. IR 1200/1250/2020/OTP B201581

Patients

Seq Age Sex Outcome Treatment
1