Defibtech, LLC: 7 recalls on record

Recalls filed with 1 agency: FDA (7).

First recall on record: June 24, 2020. Most recent: December 4, 2024.

Risk classification: Class I: 1 · Class II: 6

Most recent recalls

DateAgencyProduct
December 4, 2024FDADefibtech DDP-2002: Pediatric Defibrillation Pads For use with AED Models: Lifeline View…Z-0505-2025
December 4, 2024FDADefibtech DDP-2001: Adult Defibrillation Pads For use with AED Models: Lifeline View Aut…Z-0504-2025
December 4, 2024FDADefibtech DDP-200P: Pediatric Defibrillation Pads 0 For use with AED Models: Lifeline and…Z-0503-2025
December 4, 2024FDADefibtech DDP-100 Adult Defibrillation Pads For use with AED Models: Lifeline and Lifelin…Z-0502-2025
August 21, 2024FDARMU-2000 Automated Chest Compression DeviceZ-2543-2024
June 24, 2020FDADDU-2300 Lifeline/ReviveR View, Model Numbers DDU-C2300EN, DDU-C2300CA, DDU-A2300EN, DDU-…Z-2392-2020
June 24, 2020FDADDU-2450 Lifeline ECG Model Numbers DDU-A2450EN DDU-E2450DE DDU-E2450EN DDU-E2450FR…Z-2394-2020

Questions about this company

How many recalls does Defibtech, LLC have?
Recalert has 7 U.S. recalls on record for Defibtech, LLC, published between June 24, 2020 and December 4, 2024.
What was the most recent Defibtech, LLC recall?
FDA recall Z-0505-2025, published December 4, 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 sudde…
Which agencies have handled Defibtech, LLC recalls?
Defibtech, LLC appears as the recalling firm in recalls from: FDA (7).

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