FDA Adverse Event Malfunction Summary report: N

CONTOUR® TS

MDR report key: 22861774 · Received August 21, 2025

Report

Report Number
1810909-2025-00123
Event Type
Malfunction
Date Received
August 21, 2025
Date of Event
July 27, 2025
Report Date
August 21, 2025
Manufacturer
ASCENSIA DIABETES CARE US INC.
Product Code
NBW
PMA / PMN Number
K062058
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MX
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 0

SINCE NO PRODUCT INFORMATION WAS PROVIDED AND THE DEVICE IS NOT EXPECTED TO BE RETURNED FOR EVALUATION, NO TESTING COULD BE PERFORMED AND A DEVICE HISTORY RECORD COULD NOT BE REVIEWED. THE REPORTER INFORMATION (E1) WAS NOT PROVIDED. NO INFORMATION WAS CAPTURED IN SECTIONS A1, A2, A3 AND A4 AS THE CUSTOMER'S INITIALS, AGE, SEX AND WEIGHT WERE NOT PROVIDED. THE CUSTOMER DID NOT PROVIDE THE PRODUCT INFORMATION FOR THE CONTOUR® TS TEST STRIPS, THEREFORE NO INFORMATION WAS CAPTURED IN SECTION D4 (MODEL #, CATALOG #, LOT # AND EXPIRATION DATE), AND THE DEVICE MANUFACTURE DATE (H4) COULD NOT BE DETERMINED. THE CONTOUR® TS TEST STRIP IS SIMILAR TO THE CONTOUR® TEST STRIP AVAILABLE IN THE US MARKET. THEREFORE, PRODUCT CODE NBW AND MOST RECENT 510 (K) # K062058 ASSOCIATED WITH THE CONTOUR® TEST STRIP MARKETED IN US WERE CAPTURED IN SECTIONS D2B AND G4 RESPECTIVELY. THE DEVICE WAS DISTRIBUTED OUTSIDE THE US, THEREFORE, NO GUDID INFORMATION EXISTS.

Description of Event or Problem · 0

THE CUSTOMER FROM MEXICO REPORTED THAT THEY OPENED A BOX OF THE CONTOUR® TS TEST STRIPS AND THE BOTTLE WAS ALREADY OPEN WITH THE STRIPS BEING OUTSIDE THE BOTTLE. THERE WAS NO ALLEGATION OF AN ADVERSE EVENT. THE DEVICE IS NOT EXPECTED TO BE RETURNED FOR EVALUATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
466285 CONTOUR® TS BLOOD GLUCOSE TEST STRIPS NBW ASCENSIA DIABETES CARE US INC.

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown