Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K234065 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| CDI OneView System BPM Probe: Cat. No. CDI753 - CDI OneView BPM Probe, Cat. No. CDI753TK - CDI O... | 2 | 06/24/2025 |
FEI # 1828100 Terumo Cardiovascular Systems Corporation |
| Terumo CDI OneView Monitoring System Hematocrit / Oxygen Saturation Probe, Catalog Number REF CD1754 | 2 | 03/31/2025 |
FEI # 1828100 Terumo Cardiovascular Systems Corporation |
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