Luminex Corporation: Medical Device Recalls in 2018

According to to data from the FDA, there were 2 medical device recalls made by Luminex Corporation in 2018. See the details of the recalls below.

You can see similar recalls for other firms.

• VERIGENE Blood Culture Gram-Positive Nucleic Acid Kits (packaged as five-pack carriers) Product Usage: In vitro diagnostic test for the simultaneous detection and identification of potentially pathogenic gram-positive bacteria.
• Verigene Enteric Pathogens Nucleic Acid Test (EP) for detecting and identification of pathogenic enteric bacteria, viruses, and genetic virulence markers from liquid or soft stool preserved in Cary-Blair medium, collected from individuals with signs and symptoms of gastrointestinal infection.