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U.S. Department of Health and Human Services

Medical Device Recalls
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Related Medical Device Recalls
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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Z-0914-2017 - Prestilix 2 12/23/2016 FEI # 2126677
GE Healthcare, LLC
Z-0915-2017 - RFX 2 12/23/2016 FEI # 2126677
GE Healthcare, LLC
Z-0916-2017 - SFX 2 12/23/2016 FEI # 2126677
GE Healthcare, LLC
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