Reported Oct 14, 2026 · Ongoing · Updated Oct 20, 2026
SEDIPLAST; Model/Catalog Numbers: S-100 and S-1000;
Polymedco, Inc. / Polymedco Cancer Diagnostic Products, LLC
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: POLYMEDCO, INC. / POLYMEDCO CANCER DIAGNOSTIC PRODUCTS, LLC · 510 Furnace Dock Rd · Cortlandt Manor, NY · 10567-6220
Is this the product you have?
- SEDIPLAST
- Model/Catalog NumbersS-100 and S-1000
- Lot codes and dates
- Model/Catalog No. S-100 and S-1000
- UDI-DI
N/ALot Number E1150AExpiration Date 06/30/27
- Amount recalled
- 448400
Where it was sold
Why it was recalled
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).
This product could cause temporary or reversible health problems — stop using it.
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