Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K213668 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| SIGNA Hero, with affected software versions: PX29.1, MR30.0, MR30.1; Nuclear Magnetic Resonance Ima... | 2 | 08/02/2024 | GE Medical Systems, LLC |
| GE SIGNA Hero, Nuclear Magnetic Resonance Imaging System | 2 | 08/13/2025 | GE Medical Systems, LLC |
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