Beckman Coulter Ireland Inc
LISMEEHAN, O CALLAGHANS MILLS Clare, IE
Registered product codes
100 product codes
Recent MDR events
70 on file
- UNICEL DXH 560 AL COULTER CELLULAR ANALYSIS SYSTEMJun 16, 2026Malfunction1061932-2026-00010
- UNICEL DXH 560 AL COULTER CELLULAR ANALYSIS SYSTEMJun 16, 2026Malfunction1061932-2026-00011
- UNICEL DXH 520 COULTER CELLULAR ANALYSIS SYSTEMFeb 10, 2026Malfunction1061932-2026-00006
- UNICEL DXH 520 COULTER CELLULAR ANALYSIS SYSTEMFeb 3, 2026Malfunction1061932-2026-00004
- UNICEL DXH 560 COULTER CELLULAR ANALYSIS SYSTEMJan 7, 2026Malfunction1061932-2026-00002
- UNICEL DXH 560 COULTER CELLULAR ANALYSIS SYSTEMOct 8, 2025Malfunction1061932-2025-00030
- UNICEL DXH 560 AL COULTER CELLULAR ANALYSIS SYSTEMSep 11, 2025Malfunction1061932-2025-00027
- DXU 840M IRIS AUTOMATED URINE MICROSCOPY ANALYZERSep 5, 2025Injury2122870-2025-00095
- AQUIOS CL FLOW CYTOMETERJul 8, 2025Malfunction1061932-2025-00025
- DXH 500 HEMATOLOGY ANALYZERMay 20, 2025Malfunction1061932-2025-00024
Recalls
3 on file
- Open, ClassifiedJan 21, 2026
Beckman Coulter identified that LDL Cholesterol OSR6x96 is not meeting the performance claim listed in the Instructions for Use (IFU). LDL Cholesterol reagent showed clinically significant interference due to triglyceride concentration up to 1500 mg/dL may cause a maximum positive bias of up to 28.8% in low LDL Cholesterol samples (concentration 80 mg/dL) and up to 11.02% in high LDL Cholesterol samples (concentration 160mg/dL).
View FDA record ↗ - Open, ClassifiedDec 23, 2025
Bicarbonate reagent may generate falsely high Bicarbonate results due to interference with Lactate Dehydrogenase (LDH) in the test sample.
View FDA record ↗ - Open, ClassifiedMay 23, 2025
The product Value Assignment Sheet (VAS) is used in calibration of the device. An erroneous value was included in the VAS which has the potential to generate an incorrect APO B patient result which could exceed the total allowable error for the APO B assay (11.6%). The error results in results with a positive bias up to 42%. However, based on the mitigating factors the risk to health is considered to be negligible or limited.
View FDA record ↗
Compliance history
Matched by FEI 1000206808.
FDA inspections
0 on file
No inspections on file for this FEI number.
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.