Medical Device Recalls
-
|
11 to 15 of 15 Results
510(K) Number: K070398 |
Results per Page |
|
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
|---|---|---|---|
| The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of ... | 2 | 07/07/2017 |
FEI # 3013319212 ICU |
| The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of ... | 2 | 07/07/2017 |
FEI # 3013319212 ICU |
| The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of ... | 2 | 07/07/2017 |
FEI # 3013319212 ICU |
| Replacement Battery List Number SUB0000594 found in Plum A+ & Plum A+3 Infusion Systems, List Number... | 1 | 05/16/2023 |
FEI # 3013319212 ICU Medical Inc |
| Replacement Battery List Number SUB0000594 and SUB0000864 found in Plum A+ & Plum A+3 Infusion Syste... | 1 | 08/09/2024 |
FEI # 3013319212 ICU Medical Inc |
-







