FDA Adverse Event Malfunction Summary report: N

ACCU-CHEK GUIDE TEST STRIPS

MDR report key: 12023704 · Received June 18, 2021

Report

Report Number
3011393376-2021-01860
Event Type
Malfunction
Date Received
June 18, 2021
Date of Event
June 6, 2021
Report Date
July 1, 2021
Manufacturer
ROCHE DIABETES CARE, INC.
Product Code
NBW
UDI-DI
00365702719101
PMA / PMN Number
K160944
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

IT WAS REPORTED THE PATIENT RECEIVED THE FOLLOWING RESULTS WITHIN 15 MINUTES ON (B)(6) 2021: 379 MG/DL, 140 MG/DL AND 134 MG/DL. ON (B)(6) 2021, THE CUSTOMER RECEIVED READINGS OF 56 MG/DL, 118 MG/DL AND 140 MG/DL WITHIN 15 MINUTES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
925213 ACCU-CHEK GUIDE TEST STRIPS BLOOD GLUCOSE MONITORING TEST STRIPS NBW ROCHE DIABETES CARE, INC. 08256292001 101720 00365702719101

Patients

Seq Age Sex Outcome Treatment
1 65 YR