Recall record at a glance
| Official record | Z-2957-2026 |
|---|---|
| Category | Medical Device Recalls |
| Classification | Class II |
| FDA record status | Ongoing |
| Recalling firm | Kico Knee Innovation Company |
| Report date | Aug 26, 2026 |
| Recall initiation date | Jul 13, 2026 |
| Quantity | 78 |
| Location | Pymble, Australia |
Official product description
Brand Name: Kico Knee Innovation Product Name: ARVIS SURGICAL NAVIGATION SYSTEM GEN 2 Model/Catalog Number: IN-29200 Software Version: ARVIS Hip and Knee Gap Balance Software v3.3.2 (IN-28200) ARVIS Shoulder Software v2.0.3 (IN-23630) Product Description: The ARVIS system is a computer-controlled navigation system intended to provide intra-operative measurements to the surgeon to aid in selection and positioning of orthopedic implant components. The ARVIS Surgical Navigation System is indicated for assisting the surgeon in the positioning and alignment of implants relative to reference alignment axes and landmarks in stereotactic orthopedic surgery. The system aids the surgeon in making intraoperative measurements such as changes in leg length in Hip Arthroplasty. The system is compatible with straight acetabular impactors and with specific offset impactors, identified in the instructions for use, for which an adapter has been validated. Example orthopedic surgical procedures include but are not limited to: " Total Knee Arthroplasty " Unicompartmental Knee Arthroplasty: Tibial Transverse Resection " Hip Arthroplasty The ARVIS" head mounted display is for displaying augmented reality visualization and information to the user intraoperatively. The augmented/virtual displayed information should not be relied upon solely for absolute positional/alignment information and should always be used in conjunction with the displayed stereotaxic information. Component: NA
Why the product was recalled
Due to an internal sensor issue, image displayed with eyepiece may appear tilted relative to the eyepiece housing
Distribution information
Consignee Consignee Number Region Device Quantity RFK MEDICAL CE102 RICHMOND VA IN-29200, ARVIS SURGICAL NAVIGATION 1 VALOR MEDICAL CE118 SAN ANTONIO TX IN-29200, ARVIS SURGICAL NAVIGATION 2 JOINT VENTURES MEDICAL CE121 OSHKOSH WI IN-29200, ARVIS SURGICAL NAVIGATION 1 CASTLE MEDICAL CE122 WATERLOO IA IN-29200, ARVIS SURGICAL NAVIGATION 6 GREAT LAKES MEDICAL GL108 NAPERVILLE IL IN-29200, ARVIS SURGICAL NAVIGATION 2 CERTUS MEDICAL GL112 INDIANAPOLIS IN IN-29200, ARVIS SURGICAL NAVIGATION 5 I&S MEDICAL GL113 LOUISVILLE KY IN-29200, ARVIS SURGICAL NAVIGATION 2 PROCORE MEDICAL MA102 PIEDMONT SC IN-29200, ARVIS SURGICAL NAVIGATION 1 FOX MEDTECH MW001 ENGLEWOOD CO IN-29200, ARVIS SURGICAL NAVIGATION 2 MEDSOURCE NE131 TIVERTON RI IN-29200, ARVIS SURGICAL NAVIGATION 4 IMPLANT MEDICAL SALES NE190 HICKSVILLE NY IN-29200, ARVIS SURGICAL NAVIGATION 2 KINETIC MEDICINE NW105 OMAHA NE IN-29200, ARVIS SURGICAL NAVIGATION 4 CALSURG NW115 SANTA BARBARA CA IN-29200, ARVIS SURGICAL NAVIGATION 4 MIDWEST MEDICAL RESOURCES SC181 OVERLAND PARK KS IN-29200, ARVIS SURGICAL NAVIGATION 3 ORTHO & SURGICAL SOLUTIONS SE175 GUAYNABO PR IN-29200, ARVIS SURGICAL NAVIGATION 3 JOINT MEDICAL SOLUTIONS SE180 BIRMINGHAM AL IN-29200, ARVIS SURGICAL NAVIGATION 4 FLT ORTHOPEDICS SE216 TAMPA FL IN-29200, ARVIS SURGICAL NAVIGATION 6 MAC MEDICAL W180 GILBERT AZ IN-29200, ARVIS SURGICAL NAVIGATION 1 CP ORTHO W214 HONOLULU HI IN-29200, ARVIS SURGICAL NAVIGATION 1 UNIFIED ORTHOPEDICS W223 RIVERSIDE CA IN-29200, ARVIS SURGICAL NAVIGATION 18 MOVEMENT MEDICAL W225 SEATTLE WA IN-29200, ARVIS SURGICAL NAVIGATION 6 Total number of devices in the field 78
How to read the classification
FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Letter.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
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