Medical Device Recalls
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1 result found
510(K) Number: K071341 |
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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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Arctic Sun 5000 and Arctic Sun 2000; Intended for monitoring and controlling patient temperatures. | 2 | 02/05/2016 | C.R. Bard, Inc. |
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