11 results
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19ms
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Sources: EU EUDAMED, US FDA
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Status: Open, Classified
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Defibtech DDP-100 Adult Defibrillation Pads For use with AED Models: Lifeline and Lifeline Auto (DDU-1:XX Series)- Indicated for use on victims of sudden cardiac arrest (SCA)
FDA Recall
Open, Classified
·Defibtech, LLC·Product code MKJ·October 14, 2024
Defibtech DDP-200P: Pediatric Defibrillation Pads 0 For use with AED Models: Lifeline and Lifeline Auto (DDU-l XX Series)-Indicated for use on victims of sudden cardiac arrest (SCA.)
FDA Recall
Open, Classified
·Defibtech, LLC·Product code MKJ·October 14, 2024
Defibtech DDP-2001: Adult Defibrillation Pads For use with AED Models: Lifeline View Auto, lifeline Pro, lifeline ECG, lifeline View (DDU-2XXX Series). -Indicated for use on victims of sudden cardiac arrest (SCA.)
FDA Recall
Open, Classified
·Defibtech, LLC·Product code MKJ·October 14, 2024
Defibtech DDP-2002: Pediatric Defibrillation Pads For use with AED Models: Lifeline View Auto, lifeline Pro, Lifeline ECG, Lifeline View (DDU-2XXX Series -Indicated for use on victims of sudden cardiac arrest (SCA.)
FDA Recall
Open, Classified
·Defibtech, LLC·Product code MKJ·October 14, 2024
Automated External Defibrillators, Model DDU-2450. Item number: DCF-E2460DE (German language)
FDA Recall
Open, Classified
·Defibtech, LLC·Product code MKJ·March 18, 2025
Semi-Automated External Defibrillators; Models: DDU-100 and DDU-100E. Item numbers: DCF-E110SG-DE/1 (German language), DCF-E110SG-FR/1 (French language), DCF-E110SG-IT/1 (Italian language)
FDA Recall
Open, Classified
·Defibtech, LLC·Product code MKJ·March 18, 2025
DDU-100 Lifeline Automated External Defibrillator (AED)-Indicated for use on victims of sudden cardiac arrest
FDA Recall
Open, Classified
·Defibtech, LLC·Product code MKJ·February 14, 2023
Automated External Defibrillators, Model DDU-2200, IItem numbers: DCF-E2210-D3/1(German/English dual language), DCF-E2210-F3/1(French/English dual language)
FDA Recall
Open, Classified
·Defibtech, LLC·Product code MKJ·March 18, 2025
RMU-2000 Automated Chest Compression Device
FDA Recall
Open, Classified
·Defibtech, LLC·Product code DRM·July 12, 2024
Automated External Defibrillators, Model DDU-2300. Item numbers: DCF-E2310D3/1(German/English dual language), DCF-E2310E3/1(German/French dual language), DCF-E2310F3/1 (French/English dual language), DCF-E2310G3/1(French/German dual language), DCF-E2310IT (Italian language)
FDA Recall
Open, Classified
·Defibtech, LLC·Product code MKJ·March 18, 2025
Automated External Defibrillators, Model DDU-2200, IItem numbers: DCF-E2210-D3/1(German/English dual language), DCF-E2210-F3/1(French/English dual language)
FDA Recall
Open, Classified
·Defibtech, LLC·Product code MKJ·March 18, 2025