Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K150087 |
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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 Vivid Ultrasound products, Model Numbers: a) Vivid E90, H45581LB; b) Vivid E95, H45581DA | 2 | 07/05/2024 | GE Vingmed Ultrasound As |
GE Vivid E80 ultrasound system Vivid E80 / E90 / E95 ultrasound system is general-purpose ultraso... | 2 | 09/06/2018 | GE Medical Systems Ultrasound & Primary Care Diagnostics, LL |
GE Vivid E95 ultrasound system Product The device is intended for use by a qualified physician fo... | 2 | 09/06/2018 | GE Medical Systems Ultrasound & Primary Care Diagnostics, LL |
GE Vivid E90 ultrasound system Product Usage: Vivid E80 / E90 / E95 ultrasound system is general-... | 2 | 09/06/2018 | GE Medical Systems Ultrasound & Primary Care Diagnostics, LL |
Vivid E95/E90/E80, H45581DC, H45581LB and H45581DA. | 2 | 04/11/2017 | GE Healthcare, LLC |
Vivid S60/S70/S60N/S70N, H45041SU, H45041SW, H45581MS, H45581PD. | 2 | 04/11/2017 | GE Healthcare, LLC |
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