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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K062361
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a. McKesson Rapid Test Kit McKesson Consult Fertility Test hCG Pregnancy Test Serum / Urine Sample 2... 2 08/26/2022 FEI # 3004386693
Mckesson Medical-Surgical Inc. Corporate Office
a. ABBOTT RAPID DX N AMERICA LLC Alere Rapid Test Kit Alere Fertility Test hCG Pregnancy Test Urine ... 2 08/26/2022 FEI # 3004386693
Mckesson Medical-Surgical Inc. Corporate Office
Alere" hCG Combo Cassette (20/10 mIU/mL) Kit. Product Usage: The AlereTM hCG Combo (20/10 mIU/... 2 05/25/2013 FEI # 1000125596
Alere San Diego, Inc.
Fisher Healthcare Sure-Vue Serum/Urine hCG-STAT; in vitro diagnostic test; Catalog Number: FHC-A202;... 2 05/06/2008 FEI # 3005689981
Innovacon Inc
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