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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 42 Results
Related Medical Device Recalls
 
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Product Description
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Class
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FDA Recall
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Z-0613-2020 - C7000 - CUSA® Clarity Ultrasonic Tissue Ablation System 2 12/08/2019 Integra LifeSciences Corp.
Z-0654-2020 - C7000 - CUSA® Clarity Ultrasonic Tissue Ablation System 2 12/08/2019 Integra LifeSciences Corp.
Z-0615-2020 - C7000 - CUSA® Clarity Ultrasonic Tissue Ablation System 2 12/08/2019 Integra LifeSciences Corp.
Z-0616-2020 - C7000 - CUSA® Clarity Ultrasonic Tissue Ablation System 2 12/08/2019 Integra LifeSciences Corp.
Z-0617-2020 - C7000 - CUSA® Clarity Ultrasonic Tissue Ablation System 2 12/08/2019 Integra LifeSciences Corp.
Z-0618-2020 - C7000 - CUSA® Clarity Ultrasonic Tissue Ablation System 2 12/08/2019 Integra LifeSciences Corp.
Z-0619-2020 - C7000 - CUSA® Clarity Ultrasonic Tissue Ablation System 2 12/08/2019 Integra LifeSciences Corp.
Z-0620-2020 - C7000 - CUSA® Clarity Ultrasonic Tissue Ablation System 2 12/08/2019 Integra LifeSciences Corp.
Z-0621-2020 - C7000 - CUSA® Clarity Ultrasonic Tissue Ablation System 2 12/08/2019 Integra LifeSciences Corp.
Z-0622-2020 - C7000 - CUSA® Clarity Ultrasonic Tissue Ablation System 2 12/08/2019 Integra LifeSciences Corp.
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