FDA Medical devices recall ·

Access PCT Reagent Pack recall

Recall number
Z-1112-2025
Date
(initiated January 2, 2025)
Company / brand
Beckman Coulter, Inc.
250 S Kraemer Blvd, Brea, CA, United States
Category
Medical devices › Class II
Classification
Class II
Status
Ongoing
Units affected
6,994 US; 10,067 OUS
Initiated by
Voluntary: Firm initiated

Read the official FDA notice ↗

Product

Access PCT Reagent Pack, Catalog Number C53987, when used on Access 2 and UniCel Dxl Immunoassay Systems

Why was it recalled?

Identified reagent lots are experiencing a high rate of calibration failures with failure code of "Max Iterate" on Access 2 and UniCel Dxl Immunoassay Systems. Reporting of results may be delayed due to the time required to achieve a passing calibration curve.

What should you do?

FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.

Product codes & lot numbers

UDI-DI 15099590736002 Lots 339062, 439811

Distribution

Worldwide distribution - US Nationwide and the countries of Austria, Bahrain, Bangladesh, Belgium, Bosnia and Herzegovina, Brazil, Canada, Chile, China, Croatia, Czechia, Denmark, France, Germany, Greece, Hungary, India, Ireland, Italy, Kazakhstan, Korea, Republic of, Malaysia, Mexico, Peru, Philippines, Poland, Puerto Rico, Romania, Slovakia, South Africa, Spain, Switzerland, Thailand, Tunisia, Turkey, United Arab Emirates, United Kingdom of Great Britain and Northern Ireland, Viet Nam.

States: Puerto Rico

What does Class II mean?

Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.

Source: FDA (medical devices), recall Z-1112-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.