Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K143345 |
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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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SIGNA Pioneer, with affected software versions: PX25.0 to PX25.5, PX26.0, PX26.1, PX28.0 to PX28.4,... | 2 | 08/02/2024 | GE Medical Systems, LLC |
GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA Pioneer System, nuclear... | 2 | 02/09/2022 | GE Healthcare, LLC |
SIGNA Pioneer nuclear magnetic resonance imaging system | 2 | 10/16/2021 | GE Healthcare, LLC |
SIGNA Pioneer - Product Usage: is a whole body magnetic resonance scanner designed to support high r... | 2 | 07/12/2021 | GE Healthcare, LLC |
SIGNA Pioneer Nuclear Magnetic Resonance Imaging System - Product Usage: is a whole body magnetic re... | 2 | 01/28/2020 | GE Healthcare, LLC |
SIGNA Pioneer MR Systems Product Usage: The SIGNA Pioneer is a whole body magnetic resonance sca... | 2 | 04/07/2016 | GE Medical Systems, LLC |
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