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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: DEFIBTECH LLC LIFELINE; AUTOMATED EXTERNAL DEFIBRILATOR

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DEFIBTECH LLC LIFELINE; AUTOMATED EXTERNAL DEFIBRILATOR Back to Search Results
Model Number DDU-100
Device Problem Battery Problem (2885)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Type  malfunction  
Event Description
The customer reported that when checking aed, the defibrillator device is not working properly.The battery seems to be the issue.No additional information provided.This reported event did not occur during patient use.
 
Manufacturer Narrative
Although requested, additional information regarding the complaint has not been provided and the cause of the complaint is not known.Should additional information become available a follow-up mdr shall be submitted.
 
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Brand Name
LIFELINE
Type of Device
AUTOMATED EXTERNAL DEFIBRILATOR
Manufacturer (Section D)
DEFIBTECH LLC
741 boston post rd
suite 201
guliford 06437
Manufacturer (Section G)
DEFIBTECH LLC
14 commercial st
branford CT 06405
Manufacturer Contact
ian white
741 boston post rd
suite 201
guliford, CT 06437
2034536654
MDR Report Key19198358
MDR Text Key341417542
Report Number3003521780-2024-00369
Device Sequence Number1
Product Code MKJ
UDI-Device Identifier10815098020000
UDI-Public10815098020000
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
P160032
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Consumer
Reporter Occupation Other
Type of Report Initial
Report Date 03/27/2024
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 NumberDDU-100
Initial Date Manufacturer Received 03/27/2024
Initial Date FDA Received04/26/2024
Was Device Evaluated by Manufacturer? No
Date Device Manufactured11/07/2018
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Unknown
Patient Sequence Number1
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