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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: K131554
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RX Daytona Plus (with ISE/without ISE); Models Nos. RX4040 (w/ISE) and RX4041 (without ISE) - Produc... 2 02/24/2020 FEI # 1000361607
Randox Laboratories, Limited
RX Daytona Plus (without ISE)- IVD Clinical Chemistry Analyser (1) RX4041, (2) RX4041R (refurbished... 2 10/31/2023 FEI # 1000361607
Randox Laboratories Ltd.
RX Daytona, Model Nos. RX4040 and RX4041 2 07/25/2019 FEI # 1000361607
Randox Laboratories, Limited
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