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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-1368-2013 - CobasĀ® 8000 modular analyzer series software version 03-01, 02, 03 and 04, impacting the cobas e 602 module only. Product Usage: Fully automated immunoassay analyzer intended for the in-vitro quan... 2 May-23-2013 Roche Diagnostics Operations, Inc.
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