FDANovember 16, 2018device

Presource Kit Total Joint Pack containing a double-wrapped basin component. Product Usage: This kit is used on patients undergoing joint replacement knee or hip.

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

The hazard

The double wrapping of this custom kit basin set is not supported by the current sterility assurance validation.

What to do

FDA enforcement status: Terminated

Brands named

cardinal healthcardinal

Recall history

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

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