Beckman Coulter Ireland, Inc.: Medical Device Recall in 2025 - (Recall #: Z-1815-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.
Product Description:

Apo B Reagent, REF: OSR6143

Product Classification:

Class III

Date Initiated: April 23, 2025
Date Posted: June 4, 2025
Recall Number: Z-1815-2025
Event ID: 96746
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.

Status: Ongoing
Product Quantity: 2747 units
Code Information:

Lot # 2631/UDI: 15099590010409

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.

Voluntary or Mandated:

Voluntary: Firm initiated