Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K052978 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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GE Healthcare MR superconducting magnets, a component of GE Healthcare 1.5T SIGNA HDe MR System, nuc... | 2 | 02/09/2022 | GE Healthcare, LLC |
GE Healthcare, GE 1.5T SIGNA HDe MR SYSTEM. Indicated for use as a diagnostic imaging device. | 2 | 05/01/2013 | GE Healthcare, LLC |
Optima MR450w, Discovery MR450, Discovery MR750, Signa HDx, Signa HDxt, Signa HDi, Signa Vibrant, an... | 2 | 03/11/2013 | GE Healthcare, LLC |
4) Signa HDe (K052978 GE 1.5T Signa HDe MR System) The GE Signa® HDe MR system is a whole body... | 2 | 02/24/2011 | GE Healthcare, LLC |
Signa Excite 1.5T, Signa HD 1.5T, Signa HDx 1.5T, Signa HDxT 1.5T, Signa HDe, GE DISCOVERY MR450 and... | 2 | 01/11/2010 | GE Medical Systems, LLC |
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