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Open, Classified

Access 2 Immunoassay Analyzer, Catalog Number 81600N

FDA Recall Z-1386-2025 · Posted 2025-03-17

Recalling FirmBeckman Coulter, Inc.
Recall StatusOpen, Classified
Product CodeJJE
Date Initiated2025-02-05
Product Quantity873 units

Reason for Recall

Beckman Coulter identified that an issue for Access 2 Sample Motors (B48016) due to improper alignment, causing the motors to rub against the sample wheelbase plate and index sensor. The issue was traced to a worn tool used in production (at the supplier), affecting Access 2 sample motors. This could lead to a potential delay in reporting patient test results.

Firm Action

An URGENT MEDICAL DEVICE RECALL notification letter dated 1/31/25 was sent to customers. If the error occurs: 1. Confirm the system is in the Ready or Not Ready mode. 2. Go to the Initialize System window. To get to this window from the Main Menu, select Diagnostics F7 to display the Diagnostics menu, then select Initialize System F1. The Initialize System window is displayed with a confirmation message. 3. Select Yes F1 to initialize the instrument. Contact your Beckman Coulter representative if your laboratory has experienced sample carousel motion errors that are not resolved by initializing the analyzer. Your Beckman Coulter service representative will replace the sample motor during your next semi-annual preventative maintenance or repair visit. 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. So that we are assured you have received this important communication, please respond within 10 days in one of the following ways: Electronically, if you received this communication via email. Manually, complete and return the enclosed Response Form. If you have any questions regarding this notice, please contact our Customer Support: From our website: http://www.beckmancoulter.com

Root Cause

Nonconforming Material/Component

Distribution Pattern

Worldwide - US Nationwide 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.

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