Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K142708 |
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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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Veradius Unity, Model #718132 | 2 | 02/17/2022 | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
Veradius Unity with Software Release 2.1- Amobile, diagnostic X-ray imaging and viewing system. . M... | 2 | 12/09/2021 | Philips North America Llc |
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