Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K171128 |
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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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| SIGNA Premier systems | 2 | 04/02/2026 |
FEI # 3005326970 GE Healthcare LLC |
| GE SIGNA Premier, Nuclear Magnetic Resonance Imaging System | 2 | 08/13/2025 |
FEI # 2183553 GE Medical Systems, LLC |
| SIGNA Premier magnetic resonance scanner, model 5748519. | 2 | 07/21/2022 |
FEI # 2126677 GE Healthcare, LLC |
| GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA Premier System, nuclea... | 2 | 02/09/2022 |
FEI # 2126677 GE Healthcare, LLC |
| SIGNA Premier nuclear magnetic resonance imaging system | 2 | 10/16/2021 |
FEI # 2126677 GE Healthcare, LLC |
| SIGNA Premier - Product Usage: is a whole body magnetic resonance scanner designed to support high r... | 2 | 07/12/2021 |
FEI # 2126677 GE Healthcare, LLC |
| SIGNA Premier Nuclear Magnetic Resonance Imaging System - Product Usage: is a whole body magnetic re... | 2 | 01/28/2020 |
FEI # 2126677 GE Healthcare, LLC |
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