Medical Device Recalls
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1 result found
510(K) Number: K031749 |
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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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BodyGuard Microset For Use with the BodyGuard Infusion Pump *** Tubing: 110 in. (280 cm) - Blue Stri... | 2 | 05/04/2020 | CME America, LLC |
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