Medical Device Recalls
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1 result found
510(K) Number: K982640 |
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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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Medfusion 3500 Syringe Infusion Pump with PharmGuard Medication safety Software versions 4.1.3 and 4... | 2 | 04/26/2007 | Smiths Medical MD, Inc. |
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