Medical Device Recalls
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1 result found
510(K) Number: K133807 |
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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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MARS Treatment Kit, Use only with MARS(R) Monitor 1TC, GAMBRO, Product Code 800541 | 2 | 01/24/2018 | Baxter Healthcare Corporation |
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