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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 7 of 7 Results
Related Medical Device Recalls
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Z-2282-2019 - Aries Bordetella Assay, REF 50-10037, UDI # 00840487101452 2 08/15/2019 Luminex Corporation
Z-2283-2019 - ARIES HSV 1&2 Assay , REF 50-10017, UDI # 00840487100295 2 08/15/2019 Luminex Corporation
Z-2284-2019 - ARIES Flu A/B & RSV Assay , REF 50-10020, UDI # 00840487100158 2 08/15/2019 Luminex Corporation
Z-2288-2019 - ARIES Extraction Kit; ARIES System; SYNCT , REF 50-10026, UDI # 00840487100073 2 08/15/2019 Luminex Corporation
Z-2286-2019 - ARIES Group A Strep Assay , REF 50-10041, UDI # 00840487101469 2 08/15/2019 Luminex Corporation
Z-2287-2019 - ARIES C. difficile Assay , REF 50-10018, UDI # 00840487100059 2 08/15/2019 Luminex Corporation
Z-2285-2019 - ARIES GBS Assay , REF 50-10021, UDI # 00840487100165 2 08/15/2019 Luminex Corporation
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