Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PE Centrifuge Recalled by Beckman Coulter Biomedical GmbH Due to The adhesive joint between the plastic socket and...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Beckman Coulter Biomedical GmbH directly.
Affected Products
PE Centrifuge, REF: B36365, a component of the Power Express
Why Was This Recalled?
The adhesive joint between the plastic socket and metal component of the Power Express Sample Holder can fail, causing the metal part to detach and enter the centrifuge. This detachment can result in damage to the centrifuge and potential destruction of the patient sample resulting in delayed results and possible exposure of lab technician to biohazardous material.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Beckman Coulter Biomedical GmbH
Beckman Coulter Biomedical GmbH has 6 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report