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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 3 of 3 Results
Related Medical Device Recalls Recall Date to: 09/02/2015
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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Z-0009-2011 - GE Datex-Ohmeda Avance Anesthesia System, manufactured by GE Healthcare, P.O. Box 900, FIN-00031 GE, Finland 2 10/06/2010 GE Healthcare, LLC
Z-0010-2011 - GE Datex-Ohmeda Amingo Anesthesia System, manufactured by GE Healthcare, P.O. Box 900, FIN-00031 GE, Finland 2 10/06/2010 GE Healthcare, LLC
Z-0008-2011 - GE Datex-Ohmeda Aisys Anesthesia System, manufactured by GE Healthcare, P.O. Box 900, FIN-00031 GE, Finland 2 10/06/2010 GE Healthcare, LLC
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