FDA Adverse Event Malfunction Summary report: N

PRECISION XTRA

MDR report key: 6059320 · Received October 26, 2016

Report

Report Number
2954323-2016-06241
Event Type
Malfunction
Date Received
October 26, 2016
Date of Event
October 21, 2016
Report Date
April 3, 2017
Manufacturer
ABBOTT DIABETES CARE INC
Product Code
NBW
PMA / PMN Number
K040814
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
ES
Reporter Occupation
PATIENT

Narratives

Additional Manufacturer Narrative · 1

THIS SERVES AS A CORRECTION REPORT. SECTION D1 BRAND NAME WAS INCORRECTLY IDENTIFIED AS FREESTYLE PRECISION NEO. THE CORRECT BRAND NAME HAS BEEN UPDATED TO REFLECT THE CORRECTION. IN ADDITION SECTION G5 PMA/510K# HAS BEEN UPDATED TO K040814.

Additional Manufacturer Narrative · 1

UNLESS FURTHER INFORMATION IS OBTAINED, THIS ISSUE IS CONSIDERED CLOSED. ALL PERTINENT INFORMATION AVAILABLE TO ABBOTT DIABETES CARE HAS BEEN SUBMITTED.

Additional Manufacturer Narrative · 1

THE RETURNED METER WAS INVESTIGATED WITH RETAINED TEST STRIPS. METER POWERED ON WITH BUTTON DEPRESSION AND TEST STRIP INSERTION. NO NEW ISSUES WERE OBSERVED. BLANK SCREEN WAS NOT OBSERVED. THE COMPLAINT WAS NOT CONFIRMED.

Description of Event or Problem · 1

THE REPORTER CONTACTED ABBOTT DIABETES CARE, ALLEGING THE METER WILL NOT TURN ON. THIS COMPLAINT IS BEING REPORTED BECAUSE THE REPORTED ISSUE WAS NOT RESOLVED WITH TROUBLESHOOTING. THERE WAS NO REPORT OF DEATH, SERIOUS INJURY, OR MISTREATMENT ASSOCIATED WITH THIS EVENT.

Description of Event or Problem · 1

THE REPORTER CONTACTED ABBOTT DIABETES CARE, ALLEGING THE METER WILL NOT TURN ON. THIS COMPLAINT IS BEING REPORTED BECAUSE THE REPORTED ISSUE WAS NOT RESOLVED WITH TROUBLESHOOTING. THERE WAS NO REPORT OF DEATH, SERIOUS INJURY, OR MISTREATMENT ASSOCIATED WITH THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
709722 PRECISION XTRA BLOOD GLUCOSE MONITORING SYSTEM NBW ABBOTT DIABETES CARE INC 98814-65

Patients

Seq Age Sex Outcome Treatment
1