Kico Knee Innovation Company FDA Recalls

4 recalls on file across devices, 0 of them Class I and 4 still open. This firm is not matched to a listed company.

Newest first

Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.

Product	Reason	Class	Initiated
Brand Name: Kico Knee Innovation Product Name: ARVIS SURGICAL NAVIGATION SYSTEM GEN 2 Model/Catalog Number: IN-29200 Class IIJul 13, 2026Due to an internal sensor issue, image displayed with eyepie	Due to an internal sensor issue, image displayed with eyepiece may appear tilted relative to the eyepiece hous	Class IIDevices	Jul 13, 2026
Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the following components: IN-10500, Impactor V-BlocClass IIApr 23, 2026The V-Block Assembly and Trackers A, B, C and E may exhibit	The V-Block Assembly and Trackers A, B, C and E may exhibit signs of early wear and/or corrosion on the expose	Class IIDevices	Apr 23, 2026
Arvis Hip & Knee 2.0 Instrument Set, REF: IN-21200 containing one of the following components: IN-10500, Impactor V-BlocClass IIApr 23, 2026The Impactor V-Block Assembly and Trackers A, B, C and E may	The Impactor V-Block Assembly and Trackers A, B, C and E may exhibit signs of early wear and/or corrosion on t	Class IIDevices	Apr 23, 2026
Brand Name: ARVIS Product Name: ARVIS" Shoulder Model/Catalog Number: IN-27300, Arvis Surgical Planning Software SoftClass IISep 19, 2025Complaint identified issue with AI surgical planning softwa	Complaint identified issue with AI surgical planning software that may result in implant malalignment and/or	Class IIDevices	Sep 19, 2025