FDA Adverse Event Malfunction Summary report: N

ACCU-CHEK ® GUIDE TEST STRIPS

MDR report key: 10408172 · Received August 14, 2020

Report

Report Number
3011393376-2020-02939
Event Type
Malfunction
Date Received
August 14, 2020
Date of Event
August 4, 2020
Report Date
July 23, 2025
Manufacturer
ROCHE DIABETES CARE, INC.
Product Code
NBW
PMA / PMN Number
K160944
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MT, US
Reporter Occupation
OTHER
Health Professional
N

Narratives

Description of Event or Problem · 1

IT WAS REPORTED THE PATIENT RECEIVED THE FOLLOWING RESULTS WITHIN 15 MINUTES ON (B)(6) 2020: 38 MG/DL AND 140 MG/DL AND ON ANOTHER DAY: 29 MG/DL AND 130 MG/DL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
874164 ACCU-CHEK ® GUIDE TEST STRIPS BLOOD GLUCOSE MONITORING TEST STRIPS NBW ROCHE DIABETES CARE, INC. ASKU

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown