Beckman Coulter Biomedical GmbH: 5 recalls on record

Recalls filed with 1 agency: FDA (5).

First recall on record: September 30, 2020. Most recent: August 12, 2026.

Risk classification: Class II: 5

Most recent recalls

DateAgencyProduct
August 12, 2026FDAREMISOL Advance with Software Version 2.5 UDI-DI code: 15099590802073 The Normand Inf…Z-2834-2026
September 11, 2024FDAPE Centrifuge Temperature Controlled, REF: B36366, a component of the Power Express.Z-2980-2024
September 11, 2024FDAPower Express, REF B90918Z-2978-2024
September 11, 2024FDAPE Centrifuge, REF: B36365, a component of the Power ExpressZ-2979-2024
September 30, 2020FDADxA 5000; Catalog Number:B50516; UDI:15099590707118 - Product Usage: The DxA 5000 is a hi…Z-2983-2020

Questions about this company

How many recalls does Beckman Coulter Biomedical GmbH have?
Recalert has 5 U.S. recalls on record for Beckman Coulter Biomedical GmbH, published between September 30, 2020 and August 12, 2026.
What was the most recent Beckman Coulter Biomedical GmbH recall?
FDA recall Z-2834-2026, published August 12, 2026: REMISOL Advance with Software Version 2.5 UDI-DI code: 15099590802073 The Normand Info REMISOL Advance Data Manager collects and manages data and workflow for 128 connections
Which agencies have handled Beckman Coulter Biomedical GmbH recalls?
Beckman Coulter Biomedical GmbH appears as the recalling firm in recalls from: FDA (5).

Do you carry products from Beckman Coulter Biomedical GmbH? Check your whole catalog free against 80,000+ recalls.

Paste up to 100 UPCs or SKUs and see which ones match a CPSC, FDA, NHTSA or FSIS recall. No account needed.

Check my catalog free

Want it checked every night instead? Starter watches 500 SKUs for $29/month. See plans

Related companies