Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K141432 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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QUADROX-i Neonatal with integrated arterial filter and VHK 11000 (VKMO 11000-USA#QUADROX-i Neo.+Res... | 1 | 11/28/2018 | Maquet Cardiovascular Us Sales, Llc |
QUADROX-i Neonatal without integrated arterial filter and VHK 11000 (VKMO 10000-USA#QUADROX-i Neo.+... | 1 | 11/28/2018 | Maquet Cardiovascular Us Sales, Llc |
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