Medical Device Recalls
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11 to 16 of 16 Results
510(K) Number: K111386 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Medfusion Syringe Pump Model 4000; Software Versions V1.5.0, V1.5.1, V1.6.0, and V1.6.1 | 1 | 08/06/2020 | Smiths Medical ASD Inc. |
Medfusion Syringe Pump Model 3500, Software Version V6.0. Infusion pump. | 1 | 08/06/2020 | Smiths Medical ASD Inc. |
Medfusion Syringe Pump 4000 Series The Medfusion® Syringe Infusion Pumps are indicated for the fo... | 2 | 03/05/2018 | Smiths Medical ASD Inc. |
Medfusion Syringe Infusion Pump, containing the Barrel Clamp Guide mechanism | 2 | 08/08/2018 | Smiths Medical ASD Inc. |
Medfusion Model 4000 Syringe Infusion Pump, with software versions V1.6.0 or V1.6.1 that have implem... | 2 | 11/21/2022 | Smiths Medical ASD Inc. |
Medfusion Model 3500 and 4000 Syringe Infusion Pumps and Medfusion 3010 and 3010A Syringe Infusion P... | 2 | 02/17/2022 | Smiths Medical ASD Inc. |
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