Intellijoint Navigation System, Software Application, IJK1 (P/N 000-0547) - Product Usage recall — FDA Z-1559-2020
During total knee arthroplasty (TKA), the software may incorrectly calculate femur resection depth.
Overview of recall records associated with Intellijoint Surgical, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 2.
During total knee arthroplasty (TKA), the software may incorrectly calculate femur resection depth.
Apple has determined that, in a limited number of older generation 15-inch MacBook Pro Units, the battery may overheat and pose a fire safety risk. To date, Intellijoint has distributed,…
This page summarizes recall records in which the official source identifies Intellijoint Surgical, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.