FDAJuly 17, 2024device

PE Centrifuge Temperature Controlled, REF: B36366, a component of the Power Express.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Ongoing

Brands named

beckman coulter biomedicalbeckmanbeckman coulter

UPCs

15099590673567

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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