FDA Adverse Event Malfunction Summary report: N

ANIMAS INSULIN INFUSION PUMP

MDR report key: 2210354 · Received August 12, 2011

Report

Report Number
2531779-2011-05838
Event Type
Malfunction
Date Received
August 12, 2011
Report Date
July 15, 2011
Manufacturer
ANIMAS CORPORATION
Product Code
LZG
PMA / PMN Number
K042873
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NJ, US
Reporter Occupation
PATIENT

Narratives

Additional Manufacturer Narrative · 1

THE PUMP HAS NOT BEEN RETURNED TO ANIMAS FOR EVALUATION. ANIMAS HAS CONDUCTED A REVIEW OF THE DEVICE HISTORY RECORD FOR THIS PUMP AND CONFIRMED THAT IT WAS OPERATING WITHIN REQUIRED SPECIFICATIONS AT THE TIME OF RELEASE. IF THE DEVICE IS RETURNED, AN EVALUATION SHALL BE COMPLETED AND A SUPPLEMENTAL REPORT WILL BE FILED. NO CONCLUSIONS CAN BE MADE AT THIS TIME.

Additional Manufacturer Narrative · 1

FOLLOW-UP #1: DATE OF SUBMISSION 09/29/2015. DEVICE EVALUATION: THE DEVICE HAS BEEN RETURNED AND EVALUATED BY PRODUCT ANALYSIS ON 09/11/2015 WITH THE FOLLOWING FINDINGS: DURING A VISUAL INSPECTION OF THE KEYPAD, IT WAS NOTED THAT ALL OF THE BUTTONS WERE WORN. ALL OF THE BUTTONS ON THE KEYPAD WERE INTERMITTENTLY RESPONSIVE. THE KEYPAD COVER WAS REMOVED AND ALL OF THE BUTTON CONTACTS HAD CONTAMINATION UNDERNEATH THEM. UNRELATED TO THE ORIGINAL COMPLAINT IT WAS NOTED THAT THE DISPLAY WAS DIM AND DISCOLORED WHEN POWERED ON.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE KEYPAD BUTTON PRESSES DID NOT ACTIVATE DESIRED PUMP FUNCTIONS. THE REPORTER CLAIMED THE DOWN ARROW KEYPAD REQUIRED ADDITIONAL PRESSES WITH MORE FORCE TO RESPOND. THERE WAS NO REPORTED PATIENT IMPACT 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 CORPORATION ANM 2020 INSULIN INFUSION PUMP

Patients

Seq Age Sex Outcome Treatment
1 9 YR