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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K974059
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Product Description
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Recall
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FDA Recall
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Am I Pregnant? One Step HCG Pregnancy Test REF 100-17 2 10/23/2023 Universal Meditech Inc.
DiagnosUS Pregnancy Test Midstream REF 100-17 2 10/23/2023 Universal Meditech Inc.
PrestiBio Rapid Detection Pregnancy Test Midstream REF 100-17 3 TESTS 2 10/23/2023 Universal Meditech Inc.
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