Beckman Coulter Biomedical GmbH: Medical Device Recalls in 2020

According to to data from the FDA, there was 1 medical device recall made by Beckman Coulter Biomedical GmbH in 2020. See the detail of the recall below.

You can see similar recalls for other firms.

• DxA 5000; Catalog Number:B50516; UDI:15099590707118 - Product Usage: The DxA 5000 is a high-speed, modular, automated sample handling system that performs pre-analytical and post-analytical sample processing and storage. The automation system also sorts, routes, and presents sample tubes to analyzers for analysis. The DxA 5000 also consolidates a variety of analytical instruments, such as an Immunoassay analyzer, into a unified workstation on a track system.