Orthopedic implants are complex systems made up of several components. Our dedicated surgeons have a wealth of options to choose from to best accommodate their patients' needs. However, this complexity can give rise to significant challenges. Manufacturers establish stringent rules for the assembly of these implant components, and these specifications are meticulously detailed in compatibility tables.

Due to the high degree of modularity in orthopedic implant systems, the complexity escalates, making the chances of mismatches a concern. Operating without the manufacturer's approval, such mistakes fall onto the surgeon's responsibility and liability.

In 2006, a report revealed a distressing series of events where 47 consecutive patients in Germany received erroneously implanted total knee implants due to translation errors on the packaging, misinformation, and lack of control mechanisms. This led to 30 adverse events requiring revisions¹.

The repercussions of these mistakes are not only medical but also financial. In the US alone, the annual cost to hospitals for such errors is projected to reach $112,033,000 by 2030². Moreover, implant waste, which occurred in 2% of 3443 procedures, had an annualized cost of $109,295.35, with 67% of this cost absorbed by the hospitals themselves.