FDAFebruary 11, 2020device

Intellijoint Navigation System, Software Application, IJK1 (P/N 000-0547) - Product Usage: The Intellijoint Navigation System is a computer-controlled, optical localizer intended to provide intra-operative measurements to a surgeon to aid in selection and positioning of orthopedic implant system ...

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

The hazard

During total knee arthroplasty (TKA), the software may incorrectly calculate femur resection depth.

What to do

FDA enforcement status: Terminated

Brands named

intellijoint surgicalintellijoint

Recall history

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

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Intellijoint Navigation System, Software Application, IJK1 (P/N 000-0547) - Product Usage: The Intellijoint Navigation System is a computer-controlled, optical localizer intended to provide intra-operative measurements to a surgeon to aid in selection and positioning of orthopedic implant system ... — Recall Details · AllClear