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Beckman Coulter Biomedical GmbH recalls PE Centrifuge, REF: B36365, a component of the Power Express
Recalled September 11, 2024 · FDA recall Z-2979-2024 · Beckman Coulter Biomedical
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. · FDA Class II
Sold at
Worldwide distribution - US Nationwide and the countries of Australia, Bahrain, Canada, China, Colombia, Egypt, France, Germany, Italy, Jordan, Korea, Kuwait, Lebanon, Malaysia, Panama, Qatar, Russian Federation, Saudi Arabia, Singapore, Spain, Taiwan, Thailand, Turkey, United Arab Amirates, United Kingdom, Vietnam.
Description
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.
Product
PE Centrifuge, REF: B36365, a component of the Power Express
Manufacturer(s)
Beckman Coulter Biomedical GmbH
Made in
Germany
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →