FDAJanuary 21, 2020device

COLUMBUS CRA/PSA TIB.PLAT.CEMENTED, Knee implant components, various sizes, model nos. NN469K NN470K NN471K NN472K NN473K NN474K NN475K NN476K NN477K NN478K NN479K Product Usage: Tibia-Plateaus are part of implants in the group of knee endoprosthetics. For these implant parts there are cemented a...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Low Density Polyethylene (LDPE) particles may be present on the surface of the implant upon the opening of the inner packaging.

What to do

FDA enforcement status: Terminated

Brands named

aesculap implant systemsaesculapaesculap implant

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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