FDA Adverse Event Malfunction Summary report: N

ONETOUCHPING GLUCOSEMGMTSYSTEM

MDR report key: 3890728 · Received June 24, 2014

Report

Report Number
2531779-2014-18081
Event Type
Malfunction
Date Received
June 24, 2014
Report Date
June 19, 2014
Manufacturer
ANIMAS CORPORATION
Product Code
LZG
PMA / PMN Number
K080639
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TN, US
Reporter Occupation
PATIENT

Narratives

Additional Manufacturer Narrative · 1

FOLLOW-UP #1: DATE OF SUBMISSION 07/31/2014 DEVICE EVALUATION: THE DEVICE HAS BEEN RETURNED AND EVALUATED BY PRODUCT ANALYSIS ON (B)(4) 2014 WITH THE FOLLOWING FINDINGS: NO DEFECT WAS FOUND. PUMP POWERS WITH RETURNED BATTERY CAP. BATTERY CAP IS ABLE TO FULLY TIGHTEN. BATTERY COMPARTMENT INTACT. TWO LOW BATTERY WARNINGS OBSERVED IN ALARM HISTORY. N REPLACE BATTERY ALARM OBSERVED IN BLACK BOX ON (B)(6) 2014 HOWEVER ONE REPLACE CARTRIDGE ALARM WAS OBSERVED ON (B)(6) 2014. CONNECTED PUMP TO AN EXTERNAL POWER SUPPLY AND SLOWLY LOWERED THE INPUT VOLTAGE BELOW THE LOW BATTERY WARNING THRESHOLD, PUMP ALARMED WITH A LOW BATTERY WARNING. REMOVED PUMP CASE. NO EVIDENCE OF MOISTURE OR LOOSE COMPONENTS INSIDE PUMP.

Additional Manufacturer Narrative · 1

THE PUMP HAS NOT BEEN RETURNED TO ANIMAS FOR EVALUATION. 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.

Description of Event or Problem · 1

ON (B)(6) 2014, THE REPORTER CONTACTED ANIMAS, ALLEGING THAT SHE HAD REPLACED THE BATTERY ON JUNE 4 AND RECEIVED REPLACE BATTERY ALARM TODAY. THE PUMP DID NOT EMIT A LOW BATTERY ALARM. PATIENT IS SURE PUMP SAID REPLACE BATTERY ON SCREEN TODAY. THIS COMPLAINT IS BEING REPORTED BECAUSE THE REPORTED ISSUE WAS NOT RESOLVED WITH TROUBLESHOOTING. THERE WAS NO INDICATION THAT THE PRODUCT CAUSED OR CONTRIBUTED TO AN ADVERSE EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
367698 ONETOUCHPING GLUCOSEMGMTSYSTEM INSULIN INFUSION PUMP LZG ANIMAS CORPORATION

Patients

Seq Age Sex Outcome Treatment
1 34 YR