FREESTYLE LIBRE 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 2020-03-23 for FREESTYLE LIBRE 71940-01 71940 manufactured by Abbott Diabetes Care Inc.

Event Text Entries

[186416853] The product has been requested back for investigation. A follow- up report will be submitted once additional information is obtained. The device manufacturer date for the reported sensor is unknown. The date entered is the date of the event. All pertinent information available to abbott diabetes care has been submitted.
Patient Sequence No: 1, Text Type: N, H10


[186416854] Customer reported receiving erratic readings on their adc freestyle libre sensor. Customer reported receiving readings of 51 mg/dl, 106 mg/dl and 40 mg/dl within 10 minutes. The customer reported a horizontal trend arrow at the time of the call. The results when plotted on a parkes error grid fell into the "c" zone showing the difference in values to be clinically significant. There was no report of death, serious injury, or mistreatment associated with this event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2954323-2020-02260
MDR Report Key9865553
Report SourceCONSUMER
Date Received2020-03-23
Date of Report2020-03-23
Date of Event2020-03-08
Date Mfgr Received2020-03-08
Device Manufacturer Date2020-03-08
Date Added to Maude2020-03-23
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
Generic NameFLASH GLUCOSE MONITORING SYSTEM
Product CodePZE
Date Received2020-03-23
Model Number71940-01
Catalog Number71940
OperatorLAY USER/PATIENT
Device AvailabilityN
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
10 2020-03-23

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