Medical DeviceView official recall notice →
SEDIPLAST; Model/Catalog Numbers: S-100 and S-1000;
Product
SEDIPLAST; Model/Catalog Numbers: S-100 and S-1000;
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, potentially resulting in the release of blood and exposure of the operator or surrounding work area to a biological hazard (blood).
Units affected
448400
Description
SEDIPLAST; Model/Catalog Numbers: S-100 and S-1000;