Reported Sep 11, 2024 · Ongoing
PE Centrifuge, REF: B36365, a component of the Power Express
Beckman Coulter Biomedical GmbH
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Beckman Coulter Biomedical GmbH · Sauerbruchstr. 50 · Munchen · N/A
Is this the product you have?
- PE Centrifuge
- REFB36365, a component of the Power Express
- Lot codes and dates
- UDI(01)15099590673550/ All serial numbers Lots
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
- Nationwide
Why it was 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.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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