Medical Device Recalls
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21 to 21 of 21 Results
510(K) Number: K052013 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Nuclear Magnetic Resonance Imaging System (MRI). Trace item 9896-030-14351 -1.5T Sense XL Torso coil... | 2 | 09/22/2010 | Philips Medical Systems North America Co. Phillips |
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