Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K211980 |
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Results per Page |
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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 Systems, Magnetic Resonance imaging (MRI). SIGNA Premier, SIGNA Architect, SIGNA... | 2 | 04/21/2022 | GE Healthcare, LLC |
| SIGNA Prime, with affected software versions: MR30.1; Nuclear Magnetic Resonance Imaging System | 2 | 08/02/2024 | GE Medical Systems, LLC |
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