ACCU-CHEK ? CONNECT APP

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2018-06-18 for ACCU-CHEK ? CONNECT APP manufactured by Roche Diabetes Care, Inc..

Event Text Entries

[111348919] It was unknown if the initial reporter sent a report to the fda.
Patient Sequence No: 1, Text Type: N, H10


[111348920] Caller alleges the connect app is not giving him the recommendation for his blood glucose correction and also his carbs. Caller reported the bolus adviser does not break down his bolus information into what he should take for his insulin reading and what he should take for his meal. Caller is not using the latest version of the app. Caller is also using a version of the (b)(4) which is not supported by the connect app. No adverse event reported. Back up file has been requested for evaluation and received.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3011393376-2018-02577
MDR Report Key7610137
Report SourceCONSUMER
Date Received2018-06-18
Date of Report2018-08-20
Date of Event2018-06-04
Date Mfgr Received2018-08-03
Date Added to Maude2018-06-18
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationPATIENT
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 Received2018-06-18
Lot Number2.1.3.3
ID NumberNA
OperatorLAY USER/PATIENT
Device AvailabilityN
Device AgeDA
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 2018-06-18

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.