FDA Adverse Event Malfunction Summary report: N

ACCU-CHEK AVIVA PLUS TEST STRIPS

MDR report key: 11568810 · Received March 25, 2021

Report

Report Number
3011393376-2021-00967
Event Type
Malfunction
Date Received
March 25, 2021
Date of Event
March 11, 2021
Report Date
May 4, 2021
Manufacturer
ROCHE DIABETES CARE, INC.
Product Code
NBW
UDI-DI
00365702408104
PMA / PMN Number
K101299
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NJ, 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: 87 MG/DL AND 164 MG/DL. ON (B)(6) 2021: 185 MG/DL AND 86 MG/DL.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
469382 ACCU-CHEK AVIVA PLUS TEST STRIPS BLOOD GLUCOSE MONITORING TEST STRIPS NBW ROCHE DIABETES CARE, INC. 06908268001 498734 00365702408104

Patients

Seq Age Sex Outcome Treatment
1 75 YR