Medical Device Recalls
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1 result found
510(K) Number: K914299 |
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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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3 PORT "OFF" MANIFOLD w/WASTE BAG, SYRINGE and DyePod®, Part Number (Item #) AG8049-NS, Lot # 25286... | 2 | 10/11/2012 | ICU Medical, Inc. |
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