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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
Recall Number: Z-2028-2024
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Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020 when using Tempus LS-Manual User/Operat... 2 06/06/2024 FEI # 3003832357
Remote Diagnostic Technologies Ltd.
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