FDA Adverse Event Malfunction Summary report: N

ANIMAS INSULIN INFUSION PUMP

MDR report key: 1934986 · Received December 3, 2010

Report

Report Number
2531779-2010-02719
Event Type
Malfunction
Date Received
December 3, 2010
Report Date
November 3, 2010
Manufacturer
ANIMAS CORP.
Product Code
LZG
PMA / PMN Number
K042873
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NC, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE PUMP WAS RETURNED TO ANIMAS FOR EVAL. THE RESULTS OF THE INVESTIGATION WERE AS NOTED: THE PUMP WAS RETURNED WITH THE KEYPAD LIFTING UP BELOW THE "OK" KEYPAD BUTTON. THE "UP/DOWN/OK/CONTRAST" KEYPAD BUTTONS ARE INTERMITTENTLY RESPONDING AND REQUIRE EXCESSIVE FORCE TO ACTIVATE DURING TESTING. THE KEYPAD WAS REMOVED FOR FURTHER INVESTIGATION. DURING A VISUAL INSPECTION, THE "UP/DOWN" KEY CONTACTS ARE MISALIGNED, AND THE "UP/DOWN/OK/CONTRAST" KEY CONTACTS ARE INVERTED AND DO NOT ALWAYS SPRING BACK. THERE WAS EVIDENCE OF KEYPAD ADHESIVE FOUND UNDER ALL KEY CONTACTS.

Description of Event or Problem · 1

THE LAY-USER/PT ALLEGED THAT THE BUTTON ON THE KEYPAD DO NOT RESPOND. THERE WAS PRODUCT MISUSE. THE KEYPAD DID NOT APPEAR TO BE 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 NA

Patients

Seq Age Sex Outcome Treatment
1