Beckman Coulter Ireland, Inc.: Device Recall
Recall #Z-1815-2025 · 04/23/2025
Recall Details
- Recall Number
- Z-1815-2025
- Classification
- Class III
- Product Type
- Device
- Recalling Firm
- Beckman Coulter Ireland, Inc.
- Status
- Ongoing
- Date Initiated
- 04/23/2025
- Location
- O'Callaghan'S Mills, N/A, Ireland
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2747 units
Reason for Recall
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.
Product Description
Apo B Reagent, REF: OSR6143
Distribution Pattern
Worldwide - US Nationwide distribution in the states of AZ, CA, CO, FL, GA, IL, IN, MD, MI, NJ, NY, OH, OK, OR, PA, TX, VA, WA, WV and the countries of Argentina, Australia, Belarus, Belgium, Bulgaria, Canada, China, Czechia, Egypt, Estonia, France, Germany, Ghana, Greece, Hong Kong, India, Ireland, Israel, Italy, Korea, Republic of, Malaysia, Netherlands, New Zealand, Russian Federation, Saudi Arabia, Slovakia, Spain, Switzerland, Taiwan, Province of China, United Kingdom of Great Britain and Northern Ireland, United States of America, Viet Nam.
Other Recalls by Beckman Coulter Ireland, Inc.
- Class II: Risk 12/08/2025
- Class II: Risk 10/14/2025