Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K161574 |
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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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Discovery Ml Product Usage: The systems are intended for head and whole body attenuation correc... | 2 | 06/19/2019 | GE Healthcare, LLC |
Discovery MI, labeled as Discovery DMI 15 cm 3 ring, and Discovery DMI 20cm 4 ring | 2 | 07/31/2018 | GE Healthcare, LLC |
GE Healthcare Discovery Ml X-ray system | 2 | 06/12/2017 | GE Healthcare, LLC |
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