FREESTYLE LIBRE 14 DAY 71940-01 71940

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 2020-03-26 for FREESTYLE LIBRE 14 DAY 71940-01 71940 manufactured by Abbott Diabetes Care Inc.

Event Text Entries

[185224431] The reported product is not expected to be returned as the customer discarded the product. A follow-up report will be filed if product is returned or additional information is obtained. The date of event is unknown. The date entered is the date abbott diabetes care became aware of the event. The device mfg date is unknown. The date entered is the date abbott diabetes care became aware of the event. All pertinent information available to abbott diabetes care has been submitted.
Patient Sequence No: 1, Text Type: N, H10


[185224432] Customer reported experiencing a skin reaction while wearing an adc freestyle libre sensor and experienced symptoms described as "contact dermatitis and itching". Customer had contact with a healthcare professional and received clobetasol propionate 0. 05% and zyrtec for treatment. Customer additionally reported that he used torbot skin tac and mastisol to secure the sensor. There was no report of death or permanent injury associated with this event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2954323-2020-02323
MDR Report Key9884350
Report SourceCONSUMER
Date Received2020-03-26
Date of Report2020-04-01
Date of Event2020-03-24
Date Mfgr Received2020-03-27
Device Manufacturer Date2019-12-09
Date Added to Maude2020-03-26
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactTARA WILLIAMSON
Manufacturer Street1360 SOUTH LOOP ROAD
Manufacturer CityALAMEDA CA 945027001
Manufacturer CountryUS
Manufacturer Postal945027001
Manufacturer Phone5108644472
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameFREESTYLE LIBRE 14 DAY
Generic NameFLASH GLUCOSE MONITORING SYSTEM
Product CodePZE
Date Received2020-03-26
Model Number71940-01
Catalog Number71940
OperatorLAY USER/PATIENT
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerABBOTT DIABETES CARE INC
Manufacturer Address1360 SOUTH LOOP ROAD ALAMEDA CA 945027001 US 945027001


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-03-26

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