FDA Adverse Event Malfunction Summary report: N

ANIMAS INSULIN INFUSION PUMP

MDR report key: 1954345 · Received December 13, 2010

Report

Report Number
2531779-2010-02845
Event Type
Malfunction
Date Received
December 13, 2010
Report Date
October 6, 2010
Manufacturer
ANIMAS CORP.
Product Code
LZG
PMA / PMN Number
K042873
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FR
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE PUMP WAS RETURNED TO ANIMAS FOR EVAL. THE RESULTS OF THE INVESTIGATION WERE AS NOTED: KEYPAD DOES NOT SUSTAIN EXTERIOR DAMAGE. DURING A VISUAL INSPECTION, THERE WAS CONTAMINATION ACCUMULATING UNDER BUTTON CONTACTS OBSERVED.

Description of Event or Problem · 1

THE LAY-USER/PT ALLEGED THAT THE BUTTONS ON THE KEYPAD DO NOT RESPOND. THERE WAS PRODUCT MISUSE. THERE WAS NO REPORT OF THE KEYPAD BEING PEELED OR TORN. FURTHERMORE, THERE WAS NO ADVERSE EVENT ASSOCIATED WITH THIS COMPLAINT.

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