Official recall record
SEDIPLAST; Model/Catalog Numbers: S-100 and S-1000;
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2026-08-25
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Brand on record
- POLYMEDCO, INC. / POLYMEDCO CANCER DIAGNOSTIC PRODUCTS, LLC
What the authority reported
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 to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-11-05.
Record last checked against the registry on 2026-11-05.
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