Aniara Diagnostica recalls

Aniara Diagnostica appears in 11 official U.S. recall notices indexed by RecallRadar, most recently on 2026-08-12.

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

• 5-PLASMA Bivalirudin Control, Model Number 5D-44905
  FDA Device · Class II · 2026-08-12 · Aniara Diagnostica
• 5-PLASMA Bivalirudin AMR Verification Kit, Model Number 5D-45905
  FDA Device · Class II · 2026-08-12 · Aniara Diagnostica
• 5-PLASMA Bivalirudin Calibrator, Model Number 5D-46905
  FDA Device · Class II · 2026-08-12 · Aniara Diagnostica
• ZYMUTEST HIA IgG, in vitro diagnostic ELISA kit, Ref
  FDA Device · Class II · 2026-05-20 · Aniara Diagnostica
• BIOPHEN Protein C 5 kit is for in vitro quantitative determination of Protein C activity on human citrated plasma
  FDA Device · Class II · 2023-03-15 · Aniara Diagnostica
• BIOPHEN UFH Control Plasma
  FDA Device · Class III · 2022-09-21 · Aniara Diagnostica
• ZYMUTEST HIA MonoStrip, IgG ELISA kit, Model No. RK041A, for in vitro diagnostic use
  FDA Device · Class II · 2019-08-28 · Aniara Diagnostica
• ZYMUTEST HIA MonoStrip, IgGAM ELISA kit, Model No. RK041D, for in vitro diagnostic use
  FDA Device · Class II · 2019-08-28 · Aniara Diagnostica
• BIOPHEN LMWH Control C4, REF 224201
  FDA Device · Class III · 2019-04-24 · Aniara Diagnostica
• BIOPHEN UFH Control C2, REF 223901
  FDA Device · Class III · 2019-04-24 · Aniara Diagnostica
• BIOPHEN UFH Control C1, REF 224101
  FDA Device · Class III · 2019-04-24 · Aniara Diagnostica