Nanosphere recalls

Nanosphere appears in 11 official U.S. recall notices indexed by RecallRadar, most recently on 2014-10-08.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• Verigene BC-GP Kit (Catalog number 20-005-018)
  FDA Device · Class II · 2014-10-08 · Nanosphere
• Verigene BC-GN Kit (Catalog number 20-005-021)
  FDA Device · Class II · 2014-10-08 · Nanosphere
• The Verigene Enteric Pathogens Nucleic Acid Test (EP) is a multiplexed, qualitative test for simultaneous detection and identification of c…
  FDA Device · Class II · 2014-10-01 · Nanosphere
• The Verigene Gram-Positive Blood Culture Nucleic Acid Test (BC-UP) performed using the sample-to-result Verigene System is a qualitative, m…
  FDA Device · Class II · 2014-10-01 · Nanosphere
• The Verigene Gram Negative Blood Culture Nucleic Acid Test (BC-GN), performed using the sample-to-result Verigene System, is a qualitative…
  FDA Device · Class II · 2014-10-01 · Nanosphere
• The Verigene Respiratory Virus Plus Nucleic Acid Test (RV+) on the Verigene System is a qualitative nucleic acid multiplex test intended to…
  FDA Device · Class II · 2014-10-01 · Nanosphere
• The Verigene Clostridium difficile Nucleic Acid Test (CDF) is a qualitative, multiplexed in vitro diagnostic test for the rapid detection o…
  FDA Device · Class II · 2014-10-01 · Nanosphere
• Verigene CYP2C19 Nucleic Acid Test (CYP2C19 Test)
  FDA Device · Class III · 2014-09-03 · Nanosphere
• Verigene BC-GN Test Kit (Catalog number 20-005-021) includes: 1) 20 Verigene BC-GN Test Cartridges
  FDA Device · Class II · 2014-08-20 · Nanosphere
• Verigene Gram-Negative Blood Culture Nucleic Acid Test (BC-GN), performed using the sample-to-result Verigene System, is a qualitative mult…
  FDA Device · Class II · 2014-08-20 · Nanosphere
• Nanosphere Verigene Each CDF test consists of a Verigene CDF Nucleic Acid Test Kit and a Verigene CDF Amplification Reagent Kit
  FDA Device · Class III · 2014-08-20 · Nanosphere