Medical Device Recalls
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1 result found
Related Medical Device Recalls |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Z-0092-04 - Solar 8000M Patient Monitor with software versions 3A, 3B and 3C | 2 | 11/06/2003 |
FEI # 2124823 General Electric Medical Systems Information Technology |
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