FDA Adverse Event Malfunction Summary report: N

CONTOUR NEXT

MDR report key: 8953603 · Received September 2, 2019

Report

Report Number
1810909-2019-00383
Event Type
Malfunction
Date Received
September 2, 2019
Date of Event
July 31, 2019
Report Date
August 8, 2019
Manufacturer
ASCENSIA DIABETES CARE US INC.
Product Code
NBW
PMA / PMN Number
K160682
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GM
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 0

THE CUSTOMER RETURNED THE SUSPECTED CONTOUR NEXT ONE METER, WHILE THE CONTOUR NEXT TEST STRIPS (LOT # 8LPEF03A) RETURNED WAS DIFFERENT FROM THE SUSPECTED LOT OF TEST STRIPS I.E. LOT # 8BPEG18A. AN IN-HOUSE TESTING WAS PERFORMED USING THE RETURNED METER AND RETURNED TEST STRIPS. ADDITIONALLY, TESTING WAS ALSO PERFORMED USING THE RETURNED METER AND IN-HOUSE TEST STRIPS FROM LOT # 8BPEG18A. ALL READINGS WERE WITHIN SPECIFICATIONS.

Additional Manufacturer Narrative · 1

IN SOME COUNTRIES OUTSIDE THE US, CUSTOMER INFORMATION IS NOT PROVIDED DUE TO PRIVACY LAWS. NO INFORMATION WAS CAPTURED IN AS THE CUSTOMER'S AGE AND WEIGHT WERE NOT PROVIDED. THE MODEL # WAS NOT PROVIDED. THIS EVENT IS RELATED TO MDRS 1810909-2019-00384, 1810909-2019-00385, 1810909-2019-00386, 1810909-2019-00387, AND 1810909-2019-00388.

Description of Event or Problem · 1

AN ADVOCATE FROM (B)(6) REPORTED THAT WITHIN 10 MINUTES, THE CUSTOMER OBTAINED BLOOD GLUCOSE READINGS OF 396 MG/DL AND 82 MG/DL ON HIS CONTOUR NEXT ONE METER. THERE WAS NO ALLEGATION OF AN ADVERSE EVENT. THE CUSTOMER WAS ADVISED TO RETURN THE TEST STRIPS FOR EVALUATION. REPLACEMENT METER AND TEST STRIPS WERE SENT TO THE CUSTOMER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
747351 CONTOUR NEXT BLOOD GLUCOSE TEST STRIPS NBW ASCENSIA DIABETES CARE US INC. 8BPEG18A

Patients

Seq Age Sex Outcome Treatment
1