Medical Device Recalls
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1 result found
510(K) Number: K883577 |
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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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InfusO.R. Infusion Pump, an Rx syringe infusion pump; Baxter Healthcare Corporation, Deerfield, IL 6... | 3 | 02/18/2011 | Baxter Healthcare Corp. |
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