Access Testosterone assay, Catalog Number 33560
FDA Recall Z-1901-2025 · Posted 2025-06-02
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Recalling FirmBeckman Coulter, Inc.
Recall StatusOpen, Classified
Product CodeCDZ
Date Initiated2025-05-05
Product Quantity70 units
Reason for Recall
Inadequate preventative maintenance (PM)
performed on the scales of the RPL5 fill line, led to splashing (cross-contamination) between the wells of testosterone reagent packs lot 538081, which could potentially result in up to a 34% increase or a 23% decrease in patient results.
Firm Action
An URGENT MEDICAL DEVICE RECALL notification letter dated 4/23/25 was sent to customers.
ACTION:
Discontinue using and discard all remaining Access Testosterone reagent packs from the lot listed above.
Beckman Coulter recommends performing a retrospective review on patient results generated with the Access Testosterone lot listed above and assessing the need for retesting.
Contact your local Beckman Coulter representative for replacement product requests.
Beckman Coulter is no longer distributing the affected Access Testosterone reagent pack lot number and has corrected the manufacturing issue that led to cross-contamination.
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 Center:
From our website: http://www.beckmancoulter.com
If you need replacement product:
o Complete the attached Replacement Order Form and email to
[email protected] or fax to (866) 294-7850 OR
o Call Client Services at (800) 526-3821
Root Cause
Equipment maintenance
Distribution Pattern
US State: FL. UAE, Vietnam
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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