POLYMEDCO recalls

Recall found. POLYMEDCO is named in FDA Class II recall Z-0107-2027 covering SEDIPLAST. 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). Identifying details: Model/Catalog No. S-100 and S-1000; UDI-DI: N/A; Lot Number E1150A; Expiration Date 06/30/27. Status: Ongoing.

Models with recalls

SEDIPLAST (1)

All POLYMEDCO recalls

FDA Class II · Medical device · October 14, 2026

SEDIPLAST recall — POLYMEDCO, INC. / POLYMEDCO CANCER DIAGNOSTIC PRODUCTS, LLC

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 fo…

Official ID Z-0107-2027 · Official record ↗

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FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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Compiled from official public-domain government data. Last checked October 22, 2026 at 12:00 PM UTC.