Medical Device Recalls
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1 to 2 of 2 Results
Related Medical Device Recalls Recall Date to: 05/22/2015 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Z-2225-2009 - Sytec 6000, Sytec 8000, and Lemage/ProSeed/ProSpeed families. The CT/e and HiSpeed X/i families CT Scanner Systems are indicated for head and whole body X-ray Computed Tomography applications. | 2 | 09/18/2009 | GE Medical Systems, LLC |
Z-2224-2009 - GE Healthcare CT/e and HiSpeed X/i, families of computed tomography Systems with Gantry. The CT/e and HiSpeed X/i families CT Scanner Systems are indicated for head and whole body X-ray Computed To... | 2 | 09/18/2009 | GE Medical Systems, LLC |
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