Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K233107 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| This device is a digital radiography/fluoroscopy system used in a diagnostic and interventional ang... | 2 | 10/08/2025 | Canon Medical System, USA, INC. |
| Alphenix INFX-8000V, interventional fluoroscopic x-ray system | 2 | 01/27/2026 | Canon Medical System, USA, INC. |
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