MAUDE Adverse Event Report: Abbott Diabetes Care Inc FreeStyle Libre 2 Plus; Flash Glucose Monitoring System

Model Number	78747-01-0003
Medical Device Problem Code	Detachment of Device or Device Component (2907)
Health Effect - Clinical Code	Device Embedded In Tissue or Plaque (3165)
Date of Event	12/22/2025
Type of Reportable Event	Malfunction
Event or Problem Description
A customer reported that an adc device component detached and remained in skin.There was no indication that the customer required intervention from a healthcare professional to remove the component.There was no report of death, serious injury, or mistreatment associated with this event.
Additional Manufacturer Narrative
At the time of complaint intake, this event was deemed not reportable and troubleshooting determined that no further investigation of the device was required.This complaint has been reassessed as reportable upon retrospective review associated with a capa and is being submitted with all available information.All pertinent information available to abbott diabetes care has been submitted.

• Brand Name: FreeStyle Libre 2 Plus
• Common Device Name: Flash Glucose Monitoring System
• Manufacturer (Section D): Abbott Diabetes Care Inc; 1360 south loop road; alameda CA 94502 -700
• Manufacturer Contact: melissa pieplow ; 1360 south loop road; alameda, CA 94502--700 ; +1(510)384-5975
• MDR Report Key: 50817415
• Report Number: 2954323-2026-423431
• Device Sequence Number: 21385019
• Product Code: QBJ
• UDI-Device Identifier: 00357599835002
• UDI-Public: (01)00357599835002(17)2026-01-31(10)KTP012577(91)78747-01-0003
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K223435
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Consumer
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 09/18/2026

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
• Operator of Device: Lay User/Patient
• Device Model Number: 78747-01-0003
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 12/22/2025
• Initial Report FDA Received Date: 09/18/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 05/29/2025
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Patient Sex: Unknown