Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K993383 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Microstream Advance Neonatal-Infant Intubated CO2 Filter Line marketed as Adt/Pedi Intub CO2 Line ST... | 2 | 05/05/2025 | Philips North America Llc |
| Philips M3015A Microstream CO2 Extension Model No. 862393 -used with an lntelliVue X3 Patient Monit... | 2 | 07/10/2020 | Philips North America, LLC |
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