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Polymedco, Inc. / Polymedco Cancer Diagnostic Products recalls Sediplast

What should I do?

Check whether you have this device (see the product and lot details below). If you do, stop using it and contact the company or your healthcare provider for next steps.

What's the hazard?

During use of an affected tube, the operator may encounter increased resistance when inserting the pipette. The resulting pressure buildup may cause the tube cap to detach or be forcibly ejected, potentially resulting in the release of blood and exposure of the operator or surrounding work area to a biological hazard (blood).

What's affected

SEDIPLAST; Model/Catalog Numbers: S-100 and S-1000;

Read the official FDA Enforcement Report ↗