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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ABBOTT DIABETES CARE INC. FREESTYLE LIBRE 14-DAY; SENSOR, GLUCOSE, INVASIVE, NON-ADJUNCTIVE, FACTORY-CALIBRATED, USER-INITIATED

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ABBOTT DIABETES CARE INC. FREESTYLE LIBRE 14-DAY; SENSOR, GLUCOSE, INVASIVE, NON-ADJUNCTIVE, FACTORY-CALIBRATED, USER-INITIATED Back to Search Results
Lot Number 221218Q
Device Problem Material Twisted/Bent (2981)
Patient Problem Insufficient Information (4580)
Event Date 01/01/2022
Event Type  malfunction  
Event Description
Reporter calling stating that her husband has had problems with the abbott freestyle libre 14-day sensor.He was unable to apply the sensor to his arm because the needle was bent and as such it could not be used.They contacted abbott about this issue and abbott provided a new freestyle libre, however they sent a freestyle libre 2, and the libre 2 was incompatible with their glucose reader.In addition, reporter states that abbott had never provided them an appropriate usb charging cable for their reader; they have been using other usb cables to charge the reader but they plan to contact abbott to have an appropriate charging cable sent to them.Ref reports: mw5117047, mw5117048.
 
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Brand Name
FREESTYLE LIBRE 14-DAY
Type of Device
SENSOR, GLUCOSE, INVASIVE, NON-ADJUNCTIVE, FACTORY-CALIBRATED, USER-INITIATED
Manufacturer (Section D)
ABBOTT DIABETES CARE INC.
MDR Report Key16817048
MDR Text Key314128999
Report NumberMW5117046
Device Sequence Number1
Product Code PZE
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Patient Family Member or Friend
Type of Report Initial
Report Date 04/26/2023
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Device Expiration Date08/31/2023
Device Lot Number221218Q
Is the Reporter a Health Professional? No
Initial Date Manufacturer Received Not provided
Initial Date FDA Received04/26/2023
Patient Sequence Number1
Patient Age78 YR
Patient SexMale
Patient Weight102 KG
Patient EthnicityNon Hispanic
Patient RaceWhite
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