Recall StatusOpen, Classified
Date Initiated2025-08-04
Product Quantity116
Reason for Recall
On a clinical analyzer, when ordering a Clinical Chemistry (CC) combination test simultaneously with an Immunoassay (IA) test, if the IA test is processed between the CC tests, CC sample status will remain In Progress with no errors, may cause processing delays.
Firm Action
On 8/4/2025, recall notices were mailed and/or emailed to customers who were asked to do the following:
Check your software version, select Menu - About page.
- For Clinical Analyzers running software version 1.3.3 or 1.3.4, if this issue occurs, you will need to place a new order for the CC combination test,
- Select Home - Sample List task indicator, then select Active in the upper left corner of the Sample List to display samples "In Progress".
- Program the CC combination tests for these "In Progress" samples using a new rack and Sample ID, apply the new barcode, then load the rack onto the analyzer for processing.
- Set aside the rack with "In Progress" samples and contact your Beckman Coulter representative to clear them.
Firm recommends sharing the content of this letter with your laboratory and/or Medical Director.
Firm has resolved this issue in Software version 1.3.5 and a firm service representative will contact you to schedule the software upgrade.
Share this information with your laboratory staff and retain this notification as part of your laboratory Quality System documentation. If you have forwarded any of the affected product(s) listed above to another laboratory, please provide them a copy of this letter.
Complete and return the response form via email to:
[email protected]
If you have any questions regarding this product, please contact your local firm representative, or use the following link for a listing of local contact information.
https://www.beckmancoulter.com/en/support/contact-us
Root Cause
Software Design Change
Distribution Pattern
Internationally distribution to the countries of Poland, India, Dominican Republic, Lebanon, Italy, Brazil, El Salvador, Saudi Arabia, Germany, France, Nepal, Canada, Chile, Spain, Malaysia, Switzerland, Morocco, Philippines, Curacao, Qatar, United Arab Emirates, Hungary, Czechia, Oman, New Zealand, Thailand, Indonesia, Algeria, United Kingdom of Great Britain and Northern Ireland, Namibia, Turkey, Republic of Korea
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.