Sekisui Diagnostics recalls

Sekisui Diagnostics appears in 4 official U.S. recall notices indexed by RecallRadar, most recently on 2013-10-23.

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

• Product Name: OSOM C. Difficile Toxin A/B Test Catalog Numbers: 173 (for United States) and 173 E (for Europe)
  FDA Device · Class II · 2013-10-23 · Sekisui Diagnostics
• Sekisui Diagnostics, Spectrolyse PAI-1 In-Vitro Diagnostic Use for the quantitative determination of Plasminogen Activator Inhibitor Type 1…
  FDA Device · Class II · 2012-12-12 · Sekisui Diagnostics
• Sekisui Spectrolyse PAI-1, In-Vitro Diagnostic for Quantitative determination of Plasminogen Activator Inhibitor Type- 1 (PAI-1) activity i…
  FDA Device · Class II · 2012-09-26 · Sekisui Diagnostics
• MULTIGENT Acetaminophen for use with Architect/Aeroset Cat
  FDA Device · Class II · 2012-07-04 · Sekisui Diagnostics