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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 11 Results
510(K) Number: K110534
 
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Randox Laboratories Ltd. Catalogue Number CQ5052, Lot Number 4244CK (relabeled as Response Biomedica... 2 03/10/2020 Response Biomedical Corp.
Randox Liquid Cardiac Controls Catalogue Number CQ5051 2 11/15/2019 Randox Laboratories, Limited
Randox Liquid Cardiac Controls Catalogue Numbers CQ5053. 2 11/15/2019 Randox Laboratories, Limited
Randox Liquid Cardiac Controls Catalogue Number CQ5052. 2 11/15/2019 Randox Laboratories, Limited
Liquid Cardiac Control, Model Nos. CQ5051, CQ5052, CQ5053 2 06/14/2019 Randox Laboratories Ltd.
Liquid Cardiac Control, CQ5052 2 11/03/2018 Randox Laboratories Ltd.
Liquid Cardiac Control, CQ5051 2 11/03/2018 Randox Laboratories Ltd.
Liquid Cardiac Control, CQ5053 2 11/03/2018 Randox Laboratories Ltd.
Liquid Cardiac Control - Level 3, cat. no. CQ5053 Product Usage: This product is intended for in... 2 07/30/2018 Randox Laboratories Ltd.
Liquid Cardiac Control CQ5053 2 03/09/2018 Randox Laboratories, Limited
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