Every recall we track for Beckman Coulter Biomedical GmbH — 7 in all — plus the complaints and injury reports the public filed about them.
Beckman Coulter recalls REMISOL Advance software version 2.5 with UDI-DI code 15099590802073 due to incorrect combo test results. Affected users should check their software version and contact for remedy.
Beckman Coulter recalls Power Express Sample Holder (REF: B36365) due to risk of metal detachment causing sample damage and potential biohazard exposure. Affected units may have UDI: (01)15099590673550.
Beckman Coul: Power Express Sample Holders (REF B90918) may have adhesive failure causing metal detachment. This risks sample destruction and lab exposure. Affected units include all serial numbers listed.
Beckman Coulter recalls Power Express Sample Holder (REF: B36366) due to risk of metal detachment causing sample damage and potential biohazard exposure for lab technicians.
Beckman Coulter recalls DxA 5000 lab equipment due to software defect that may cause tests on incompatible patient samples, leading to erroneous results. Affected units include those with specific serial numbers and model.
Beckman Coulter recalls DxA Automation System models due to software defect that may cause incorrect patient test results. Affected units include DxA 5000 Fit with specific serial numbers. Contact for remedy details.
Beckman Coulter recalls DxA 5000 lab equipment due to unclear sample ID reuse instructions causing system failures. Affected units may need reconfiguration.
