Beckman Coulter Biomedical recalls

Beckman Coulter Biomedical appears in 7 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.

• REMISOL Advance with Software Version 2.5 UDI-DI code: 15099590802073 The Normand Info REMISOL Advance Data Manager collects and manages da…
  FDA Device · Class II · 2026-08-12 · Beckman Coulter Biomedical
• PE Centrifuge Temperature Controlled, REF: B36366, a component of the Power Express
  FDA Device · Class II · 2024-09-11 · Beckman Coulter Biomedical
• Power Express, REF B90918
  FDA Device · Class II · 2024-09-11 · Beckman Coulter Biomedical
• PE Centrifuge, REF: B36365, a component of the Power Express
  FDA Device · Class II · 2024-09-11 · Beckman Coulter Biomedical
• Beckman Coulter DxA Automation System, DxA 5000, REF: B87352, IVD, 200240V, 16A, 50/60HZ, RxOnly
  FDA Device · Class II · 2023-07-26 · Beckman Coulter Biomedical
• Beckman Coulter DxA Automation System, DxA 5000 Fit, REF: B87352, IVD, 200240V, 16A, 50/60HZ, RxOnly
  FDA Device · Class II · 2023-07-26 · Beckman Coulter Biomedical
• DxA 5000
  FDA Device · Class II · 2020-09-30 · Beckman Coulter Biomedical