Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K090785 |
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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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Phillips Charging Station, Product #: 989803191021 - Product Usage: This charging station is used in... | 2 | 08/14/2020 | Philips North America, LLC |
Phillips 3.7V Rechargeable Li-Polymer Battery, Product #: 989803191341 - Product Usage: This battery... | 2 | 08/14/2020 | Philips North America, LLC |
Phillips Module Charger, Product #: 989803191031 - Product Usage: This Module Charger is used in the... | 2 | 08/14/2020 | Philips North America, LLC |
Cardiovascular Monitoring Device accessory - Product Usage: The chest pneumograph (also referred to ... | 2 | 06/02/2020 | Philips North America, LLC |
Invivo Corporation Expression MRI Patient Monitoring System. The Expression MRI Patient Monitorin... | 2 | 12/04/2012 | Invivo Corporation |
"***Assembled for Invivo Corporation 12501 Research Parkway Orlando FL 32826***Made in U.S.A.***MRI ... | 2 | 10/25/2011 | Invivo Corporation |
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