Beckman Coulter Biomedical recalls
3 official recalls and safety alerts involving Beckman Coulter Biomedical since 2023-07, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.
This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Beckman Coulter Biomedical or the relevant agency.
- 2026-08-12
USBeckman Coulter Biomedical GmbH recalls REMISOL Advance with Software Version 2.5 UDI-DI code: 15099590802073 The Normand Info REMISOL Advance Data Manager collects and…
Due to software issues where does not handle combo assay results. The software may replace the final combo test result with one of the sub-results resulting in incorrect reporting of test outcomes.
FDA · DeviceBeckman Coulter Biomedical GmbHU.S.: FL, GA, IL, MI, and PA O.U.S.: Belgium, France, Hungary, Poland, Taiwan…Official notice →- 2024-09-11
- US
Beckman Coulter Biomedical GmbH recalls PE Centrifuge Temperature Controlled, REF: B36366, a component of the Power Express.
The adhesive joint between the plastic socket and metal component of the Power Express Sample Holder can fail, causing the metal part to detach and enter the centrifuge. This detachment can result in damage to the…
FDA · DeviceBeckman Coulter Biomedical GmbHWorldwide distribution - US Nationwide and the countries of Australia,…Official notice → - 2023-07-26
- US
Beckman Coulter Biomedical GmbH recalls Beckman Coulter DxA Automation System, DxA 5000 Fit, REF: B87352, IVD, 200240V, 16A, 50/60HZ, RxOnly
A software defect in the DxA Automation System may cause tests to be run on patient samples in tube types not compatible with the requested test, leading to erroneous patient results
FDA · DeviceBeckman Coulter Biomedical GmbHUS: AL CA FL IL IN KY MI MN MO NE NJ NV NY OH PA SC TX WI WV OUS: Australia,…Official notice →