Randox Laboratories, Limited: Medical Device Recalls in 2019

According to to data from the FDA, there were 8 medical device recalls made by Randox Laboratories, Limited in 2019. See the details of the recalls below.

You can see similar recalls for other firms.

• Assayed Bovine Multi-Sera Level 1, Model No. AL1027
• Randox Liquid Cardiac Controls Catalogue Number CQ5052.
• Human Assayed Multi-Sera Level 2, Model NO. HN1530 Product Usage: This product is intended for in vitro diagnostic use, in the quality control of diagnostic assays. The Human Assayed Multi-sera is for the control of accuracy.
• RANDOX NEFA (Non-Esterified Fatty Acids) FA115 Lot 485343, GTIN: 5055273203066.
• RX Daytona, Model Nos. RX4040 and RX4041
• RX Imola, Model Nos. RX4900
• Randox Liquid Cardiac Controls Catalogue Numbers CQ5053.
• Randox Liquid Cardiac Controls Catalogue Number CQ5051