Recalls from Aniara Diagnostica LLC

• Aniara Diagnostica 5-PLASMA Bivalirudin Kits, Calibrators and Controls (opens in a new tab)
  Moderate risk, FDA, Aug 5, 2026, Quality testing problem
• ZYMUTEST HIA IgG, in Vitro Diagnostic ELISA Kit (opens in a new tab)
  Moderate risk, FDA, May 12, 2026, Device defect

Data: Recall Canary (opens in a new tab)