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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-1587-2023 - ProxiDiagnost N90 R.1.0 2 05/15/2023 Philips North America
Z-1589-2023 - CombiDiagnost R90 R1.1 2 05/15/2023 Philips North America
Z-1588-2023 - CombiDiagnost R90 R.1.0 2 05/15/2023 Philips North America
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