Medical Device Recalls
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1 result found
510(K) Number: K061325 |
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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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CME America BodyGuard Infusion Pump System, All models of BG 323, BG 121, BG 545, BG CV545, BG 575, ... | 1 | 03/18/2020 | CME America, LLC |
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