Medical Device Recalls
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1 result found
Recall Number: Z-2279-2012 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| V Series Patient Monitors; Mindray DS USA, Inc. Product Usage: The V Series Monitor is intended ... | 2 | 08/28/2012 |
FEI # 2221819 Mindray DS USA, Inc. d.b.a. Mindray North America |
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