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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ABBOTT DIABETES CARE INC FREESTYLE LIBRE 2; FLASH GLUCOSE MONITORING SYSTEM

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ABBOTT DIABETES CARE INC FREESTYLE LIBRE 2; FLASH GLUCOSE MONITORING SYSTEM Back to Search Results
Model Number 71953-01
Device Problem Power Problem (3010)
Patient Problem Hypoglycemia (1912)
Event Date 07/17/2022
Event Type  Injury  
Manufacturer Narrative
The customer¿s product has been requested for investigation.A follow-up report will be filed once additional information is obtained.The device manufacturing 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.
 
Event Description
A customer reported a delivery issue associated with a replacement adc device.The customer initially reported experiencing an unspecified battery/power issue with the adc device and a replacement was issued.The customer indicated that due to receiving the incorrect device (freestyle libre 14 day reader instead of freestyle libre 2 reader) they were unable to set glucose alarms, as the function is not available for the freestyle libre 14 day reader.Due to this, the customer became hypoglycemic and required treatment of cola, carbohydrates, and glucose provided by a third-party.There was no report of death or permanent injury associated with this event.
 
Manufacturer Narrative
Repeated attempts by adc to retrieve the product were unsuccessful and/or the customer discarded the product.No product has been returned and a valid serial number has not been provided.Extended investigation has been performed for the reported complaint and there was no indication that the product did not meet specification.A tripped trend review was conducted for the reported complaint and libre reader, no trends were identified that would indicate any product related issues.If the product is returned, a physical investigation will be performed and a follow-up report submitted.All pertinent information available to abbott diabetes care has been submitted.
 
Event Description
A customer reported a delivery issue associated with a replacement adc device.The customer initially reported experiencing an unspecified battery/power issue with the adc device and a replacement was issued.The customer indicated that due to receiving the incorrect device (freestyle libre 14 day reader instead of freestyle libre 2 reader) they were unable to set glucose alarms, as the function is not available for the freestyle libre 14 day reader.Due to this, the customer became hypoglycemic and required treatment of cola, carbohydrates, and glucose provided by a third-party.There was no report of death or permanent injury associated with this event.
 
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Brand Name
FREESTYLE LIBRE 2
Type of Device
FLASH GLUCOSE MONITORING SYSTEM
Manufacturer (Section D)
ABBOTT DIABETES CARE INC
1360 south loop road
alameda CA 94502 7001
Manufacturer Contact
audra fuentes
1360 south loop road
alameda, CA 94502-7001
5107495297
MDR Report Key15177318
MDR Text Key297406113
Report Number2954323-2022-27629
Device Sequence Number1
Product Code QLG
Combination Product (y/n)N
Reporter Country CodeGM
PMA/PMN Number
K193371
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Consumer
Reporter Occupation Non-Healthcare Professional
Type of Report Initial,Followup
Report Date 11/09/2022
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Lay User/Patient
Device Model Number71953-01
Was Device Available for Evaluation? No
Initial Date Manufacturer Received 07/21/2022
Initial Date FDA Received08/05/2022
Supplement Dates Manufacturer Received11/02/2022
Supplement Dates FDA Received11/09/2022
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured07/21/2022
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
Patient Outcome(s) Required Intervention;
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