Every recall we track for Kico Knee Innovation Company — 4 in all — plus the complaints and injury reports the public filed about them.
Kico recalls ARVIS Surgical Navigation System Gen 2 (model IN-29200) due to potential image tilt in eyepiece. This may affect surgical alignment accuracy during procedures like knee or hip replacements.
Kico Knee Innovation recalls Arvis Hip & Knee 2.0 Instrument Set with possible early wear and corrosion on magnet faces. Affected units include specific model numbers and serial ranges. Consumers should check their instruments for signs of wear.
Kico recalls Arvis Hip & Knee 3.0 Instrument Set (REF: IN-28000) due to potential early wear and corrosion on magnet faces. Affected units include specific components and serial numbers. Consumers should check their instruments for signs of wear.
Kico Knee Innovation Company recalls ARVIS Shoulder surgical planning software version V2025.1.2 due to potential implant malalignment or reduced range of motion. Affected users should contact for remedy.
