Recall company profile

Beckman Coulter Biomedical GmbH Recalls

Overview of recall records associated with Beckman Coulter Biomedical GmbH, including dates, categories and classifications where available.

7recall records
Aug 12, 2026latest record date
Sep 30, 2020earliest record date

Recall history in this database

Classification mix: Class II: 7.

Medical DeviceSep 30, 2020

Beckman Coulter Biomedical GmbH DxA 5000 recall — FDA Z-2983-2020

The DxA 5000 instructions for use may be confusing regarding the re-use of sample IDs. Beckman Coulter has received complaints where the re-use of sample barcodes were not being detected by…

Class IIFDA: TerminatedBeckman Coulter Biomedical GmbH

Understanding this recall history

This page summarizes recall records in which the official source identifies Beckman Coulter Biomedical GmbH as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.