Luminex Corporation: Medical Device Recalls in 2021

According to to data from the FDA, there were 8 medical device recalls made by Luminex Corporation in 2021. See the details of the recalls below.

You can see similar recalls for other firms.

• Verigene Gram Negative Blood Culture Nucleic Acid Test (BC-GN) Model Number: 20-006-021
• Verigene Enteric Pathogens Nucleic Acid Test (EP) Model Number: 20-006-023
• Verigene Gram Negative Blood Culture Nucleic Acid Test v2 (BC-GNv2) Model Number: 20-006-026
• Verigene Clostridium difficile Nucleic Acid Test Kit (CDF) Model Number: 20-006-022
• Verigene Gram-Positive Blood Culture Nucleic Acid Test (BC-GP) Model Number: 20-006-018
• Verigene Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) Model Number: 20-006-024
• Verigene EP Amplification Reagent Kit Test
• VERIGENE Processor SP - Product Usage: intended for processing and identifying nucleic acids utilizing gold nanoparticle probe technology.