Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K161469 |
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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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| Replacement Battery List Number SUB0000864, found in Plum 360 Infusion System, List Number 30010 | 1 | 05/16/2023 |
FEI # 3013319212 ICU Medical Inc |
| Plum 360 Infusion System With MedNet/ Smart Card Plug And Play Module, Model # 30010. Infusion pu... | 2 | 10/22/2019 |
FEI # 3013319212 ICU Medical Inc |
| Plum 360 Infusion System, List number 30010. | 2 | 11/16/2017 |
FEI # 3013319212 ICU Medical Inc |
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