Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K190624 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| EarlyVue VS30 Vitals monitor with Software Versions A.00.02 and A.00.01 Product Number: 863380 | 2 | 05/26/2023 | Philips North America Llc |
| EarlyVue VS30 Vitals Monitor, utilizing E01 (Oridion Microstream sidestream etCO2) and R21 (Masimo R... | 2 | 09/29/2023 | Philips North America Llc |
| EarlyVue VS30 Vital Signs Monitor, utilizing E01 (Oridion Microstream sidestream etCO2) and R21 (Ma... | 2 | 09/29/2023 | Philips North America Llc |
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