Drug recall
SEDIPLAST; Model/Catalog Numbers: S-100 and S-1000;
FDA recall event 99810 · Class II · POLYMEDCO, INC. / POLYMEDCO CANCER DIAGNOSTIC PRODUCTS, LLC
Key facts
| Event ID | 99810 |
|---|---|
| Recall numbers | Z-0107-2027 |
| Recalling firm | POLYMEDCO, INC. / POLYMEDCO CANCER DIAGNOSTIC PRODUCTS, LLC |
| Product type | Devices |
| Products | SEDIPLAST; Model/Catalog Numbers: S-100 and S-1000; |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | 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… |
| Initiation date | Aug 25, 2026 |
| Report date | Oct 14, 2026 |
| City | Cortlandt Manor |
| State | NY |
| Country | United States |
| FEI number | 1000119795 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: