Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Z-0675-2018 - Cobas 8000 Modular Series system; Software Version 05-02 and 06-03; UDI: 05641446001 | 2 | 02/21/2018 | Roche Diagnostics Corporation |
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