Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K191910 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Infusomat Space Infusion System/ Large Volume Pump, Product Code 8713050U | 1 | 09/07/2024 |
FEI # 3003218564 B Braun Medical Inc |
| 8713051U, Infusomat Large Volume Pump, Wireless; Volumetric Infusion Pump System | 1 | 10/25/2023 |
FEI # 2523676 B. Braun Medical, Inc. |
| 8713052U, Infusomat Large Volume Pump, Non-Wireless BATTERY PACK; Volumetric Infusion Pump System | 1 | 10/25/2023 |
FEI # 2523676 B. Braun Medical, Inc. |
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