MAUDE Adverse Event Report: Defibtech, L.L.C. Lifeline; AUTOMATED EXTERNAL DEFIBRILLATORS

Model Number	DDU-120E
Medical Device Problem Code	Failure to Power Up (1476)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Type of Reportable Event	Malfunction
Event or Problem Description
An international distributor reported that their customer's aed was reporting a battery low warning.The customer did not report this occurring during patient use.
Additional Manufacturer Narrative
Although the customer initially reported a battery low warning, review of the aed's log files found the battery went on to fully deplete within the unit.On (b)(6) 2026, the aed identified that the aed battery was getting low and attempted to alert the user by flashing its red asi and chirping.The aed continued to flash and chirp until on (b)(6) 2026 when the battery pack became completely depleted.Analysis of the aed's log files did not identify a cause for the depleted battery.Analysis of the aed's log files identified that once a new battery was installed and a manual self test run the aed was functioning as designed and could stay in service.

• Brand Name: Lifeline
• Common Device Name: AUTOMATED EXTERNAL DEFIBRILLATORS
• Manufacturer (Section D): Defibtech, L.L.C.; 741 boston post rd.; suite 201; guilford CT 06437
• Manufacturer (Section G): Defibtech, L.L.C.; 14 commercial st.; branford
• Manufacturer Contact: nissa soto ; 741 boston post road; suite 201; guilford, CT 06437 ; +1(203)453-6654
• MDR Report Key: 50753858
• Report Number: 3003521780-2026-01432
• Device Sequence Number: 13149162
• Product Code: MKJ
• UDI-Device Identifier: 00815098020072
• UDI-Public: (01)00815098020072
• Combination Product (Y/N): N
• Initial Reporter Country: FR
• PMA/510(K) Number: P160032
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,Consumer,Distributor
• Type of Report: Initial
• Report Date (Section B): 09/14/2026

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
• Device Model Number: DDU-120E
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 08/17/2026
• Initial Report FDA Received Date: 09/14/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 06/15/2022
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Unknown
• Patient Sequence Number: 1
• Patient Sex: Unknown