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U.S. Department of Health and Human Services

Medical Device Recalls

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Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-2392-2020 - DDU-2300 Lifeline/ReviveR View, Model Numbers DDU-C2300EN, DDU-C2300CA, DDU-A2300EN, DDU-E2300EN Catalog Numbers CCD-A1006RX CCD-A1013EN CCD-A1015EN DCF-A2310EN DCF-A2310RX DCF-A2313EN DCF-C2... 2 06/17/2020 Defibtech, LLC
Z-2394-2020 - DDU-2450 Lifeline ECG Model Numbers DDU-A2450EN DDU-E2450DE DDU-E2450EN DDU-E2450FR DDU-E2450TH Cat. No. DCF-A2460EN DCF-A2463EN DCF-E2460DE DCF-E2460EN DCF-E2460FR DCF-E2460TH UDI 0... 2 06/17/2020 Defibtech, LLC
Z-2393-2020 - DDU-2400EN Lifeline PRO, UDI 00815098020270 - Product Usage: Automated External Defibrillators (AED) are indicated for use on victims of sudden cardiac arrest (SCA) who are: - unconscious and unrespon... 2 06/17/2020 Defibtech, LLC