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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 5 of 5 Results
Related Medical Device Recalls Recall Date to: 07/05/2015
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Product Description
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FDA Recall
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Z-0866-2008 - Roche/Hitachi Modular Analytics System, Modular D2400 Module GMMI clinical chemistry analyzer; Catalog number 04998618001. Intended for qualitative and quantitative in vitro determinations using a ... 2 08/13/2008 Roche Diagnostics Corp.
Z-0867-2008 - Roche/Hitachi Modular Analytics System, Modular P800 Module GMMI clinical chemistry analyzer; Catalog number 04998669001. Intended for qualitative and quantitative in vitro determinations using a w... 2 08/13/2008 Roche Diagnostics Corp.
Z-0870-2008 - Roche/Hitachi Modular Analytics System Modular P Module GMMI immunoassay analyzer; Catalog number 03284549001. Intended for qualitative and quantitative in vitro determinations using a wide variety... 2 08/13/2008 Roche Diagnostics Corp.
Z-0869-2008 - Roche/Hitachi Modular Analytics System, Modular D Module GMMI clinical chemistry analyzer; Catalog number 03284522001. Intended for qualitative and quantitative in vitro determinations using a wide... 2 08/13/2008 Roche Diagnostics Corp.
Z-0868-2008 - Roche/Hitachi Modular Analytics System, Modular E Module GMMI immunoassay analyzer; Catalog numbers 04998642001 and 03617505001. Intended for qualitative and quantitative in vitro determinations u... 2 08/13/2008 Roche Diagnostics Corp.
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