Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Open, Classified

DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137

FDA Recall Z-1326-2025 · Posted 2025-03-12

Recalling FirmBeckman Coulter, Inc.
Recall StatusOpen, Classified
Product CodeJJE
Date Initiated2024-11-13
Product Quantity245 units

Reason for Recall

The DxI 9000 Access Immunoassay Analyzer wash wheel mixer may not spin freely within the idler pulley housing. When the problem occurs, the analyzer may generate a system event for a Wash Wheel Dispense Arm Spin Mixer Error that is displayed on the navigation bar in the User Interface. The analyzer enters the red system status and will generate a SYS flag. The tests that are in progress may be cancelled and may cause a delay in reporting patient results

Firm Action

An IMPORTANT PRODUCT NOTICE letter dated 11/6/24 was sent to customers. Contact your Beckman Coulter representative if your laboratory has experienced wash wheel dispense arm spin mixer motor errors that are not resolved by initializing. See the System Management Chapter section in the DxI 9000 Access Immunoassay Analyzer Instruction for Use (IFU) for steps to initialize the Analyzer. Your Beckman Coulter service representative will contact you to schedule a part replacement that resolves this issue. Please 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 listed above to another laboratory, please provide them a copy of this letter. Please complete and return the enclosed Response Form within 10 days so we are assured you have received this important communication. If you have any questions regarding this notice, please contact our Customer Support Center: From our website: http://www.beckmancoulter.com

Root Cause

Nonconforming Material/Component

Distribution Pattern

US Nationwide. Global Distribution.

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.

↑