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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K110889
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Product Description
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Recall
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FDA Recall
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One Step Pregnancy Test REF 100-01 2 10/23/2023 FEI # 3011908678
Universal Meditech Inc.
PrestiBio Pregnancy Strips REF 100-4 25 HCG Test Strips 2 10/23/2023 FEI # 3011908678
Universal Meditech Inc.
PrestiBio Ovulation and Pregnancy Strips REF 100-4 and REF 200-4 60 LH Test Strips/+30 HCF Test Stri... 2 10/23/2023 FEI # 3011908678
Universal Meditech Inc.
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