Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K120778 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| GE Healthcare MR superconducting magnets, a component of GE Healthcare Brivo MR355 System, nuclear m... | 2 | 02/09/2022 | GE Healthcare, LLC |
| Brivo MR355, with affected software versions: SV20.3, SV23.3, MR30.0, MR30.1; Nuclear Magnetic Reso... | 2 | 08/02/2024 | GE Medical Systems, LLC |
| Optima MR360, with affected software versions: SV20.3, SV23.3, MR30.0, MR30.1; Nuclear Magnetic Res... | 2 | 08/02/2024 | GE Medical Systems, LLC |
| Brivo MR355, Optima MR360 Product Usage: The Brivo MR355/Optima MR360 is a whole body magnetic r... | 2 | 08/02/2017 | GE Medical Systems, LLC |
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