Medical Device Recalls
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1 result found
510(K) Number: K021288 |
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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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Microtek Medical, Inc. ORS Fluid Warming and Slush Drapes, Model #'s ORS-100, ORS-110, ORS-130, OR... | 2 | 09/18/2015 | Ecolab Inc |
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