ACCU-CHEK ? CONNECT APP 07250452001

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2017-10-17 for ACCU-CHEK ? CONNECT APP 07250452001 manufactured by Roche Diabetes Care, Inc..

Event Text Entries

[89753563] The event occurred outside of the united states. While this product is not sold in the united states, it is like or similar to a product marketed in the united states.
Patient Sequence No: 1, Text Type: N, H10


[89753564] Caller alleges bolus adviser in connect app gives wrong advice, it only calculates with the carbs and not with the blood glucose levels. No adverse event reported. No product will be returned.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3011393376-2017-05683
MDR Report Key6954881
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2017-10-17
Date of Report2017-10-17
Date of Event2017-09-19
Date Mfgr Received2017-10-10
Date Added to Maude2017-10-17
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationMEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactNA GREG SMITH
Manufacturer Street9115 HAGUE ROAD NA
Manufacturer CityINDIANAPOLIS IN 462500457
Manufacturer CountryUS
Manufacturer Postal462500457
Manufacturer Phone3175212484
Manufacturer G1ROCHE DIABETES CARE, INC.
Manufacturer Street9115 HAGUE ROAD NA
Manufacturer CityINDIANAPOLIS IN 462501025
Manufacturer CountryUS
Manufacturer Postal Code462501025
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameACCU-CHEK ? CONNECT APP
Generic NameDIABETES MANAGEMENT SOFTWARE
Product CodeNDC
Date Received2017-10-17
Catalog Number07250452001
Lot Number2.1.2.1
ID NumberNA
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerROCHE DIABETES CARE, INC.
Manufacturer Address9115 HAGUE ROAD NA INDIANAPOLIS IN 462500457 US 462500457


Patients

Patient NumberTreatmentOutcomeDate
10 2017-10-17

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