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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K023264
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Alaris Syringe Module Model 8110 with software version 9.15 The Alaris Syringe Pump module is par... 2 09/23/2016 FEI # 2016493
CareFusion 303, Inc.
Alaris Syringe Pump, Model 8110. The firm name on the label is CareFusion. The Alaris Syringe Pu... 2 01/08/2018 FEI # 2016493
CareFusion 303, Inc.
Alaris Syringe Pump, Model No. 8110. Delivers fluids. Expansion of Affected Units: BOM Housin... 1 08/14/2015 FEI # 2016493
CareFusion 303, Inc.
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