Medical Device Recalls
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510(K) Number: K072873 |
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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| Mammotrak Diagnostic Coil 1.5T | 2 | 11/25/2024 | Philips North America Llc |
| Mammotrak Diagnostic Coil 3.0T | 2 | 11/25/2024 | Philips North America Llc |
| dS Breast 16ch 1.5T | 2 | 11/25/2024 | Philips North America Llc |
| dS Breast 16ch 3.0T | 2 | 11/25/2024 | Philips North America Llc |
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