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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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Z-0581-2007 - Defibtech Sentry Semi-Automatic External Defibrilator (AED) sold as 'ReviveR AED' brand -Model DDU-100B (version 2.002 and earlier) 1 03/08/2007 FEI # 3003521780
Defibtech, LLC
Z-0580-2007 - Defibtech Sentry Semi-Automatic External Defibrilator (AED) sold as 'Lifeline AED' brand -Model DDU-100A (version 2.002 and earlier) 1 03/08/2007 FEI # 3003521780
Defibtech, LLC
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