Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K103327 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| System, Nuclear Magnetic Resonance Imaging - Product Usage: is a whole body magnetic resonance scann... | 2 | 10/20/2020 |
FEI # 2126677 GE Healthcare, LLC |
| GE 1.5T Signa HDxt, 3.0T Signa HDxt, Signa Vibrant, HD23 Software and the following model numbers: 2... | 2 | 09/23/2013 |
FEI # 2126677 GE Healthcare, LLC |
| GE Healthcare, Discovery MR750w 3.0T System. Part Number: 5352293. Product Usage: It is indica... | 2 | 04/11/2013 |
FEI # 2126677 GE Healthcare, LLC |
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