Kico Knee Innovation recall: Arvis Surgical Navigation System Gen 2
Kico Knee Innovation Company is recalling Arvis Surgical Navigation System Gen 2 – 78. The U.S. Food and Drug Administration published the recall on August 26, 2026; it began on July 13, 2026. Distributed in 15 states (Arizona, California, Florida, Illinois, Iowa, Kansas, Kentucky, Nebraska, New York, Puerto Rico, Rhode Island, Texas, Virginia, Washington, Wisconsin).
Serious Class II means the product may cause temporary or medically reversible health problems, or the chance of serious harm is remote.
Share
| Product | Arvis Surgical Navigation System Gen 2 |
| Brand | Kico Knee Innovation |
| Company | Kico Knee Innovation Company |
| Type | Medical devices |
| Classification | Class II |
| Recall date | July 13, 2026 |
| Published by FDA | August 26, 2026 |
| Quantity | 78 |
| Recall ID | 99372 |
Recalled products
- 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
- FDA recall number
- Z-2957-2026
- Codes, lots and dates
- Lot Code: GMDN - 45200 UDI-DI - 00810180351287 Software ARVIS Hip and Knee Gap Balance Software v3.3.2 (IN-28200) ARVIS Shoulder Software v2.0.3 (IN-23630) Serial Number 6006A1118 6006A1036C3 6006A1117 6006A1045C2 6006A1106 6006A1126 6006A1149 6006A1034C2 6006A1046C2 6006A1086C2 6006A1093 6006A1079C3 6006A1096C2 6006A1052C2 6006A1058C3 6006A1030C2 6006A1088 6006A1100C 6006A1094 6006A1041C2 6006A1060C3 6006A1092C 6006A1105 6006A1140 6006A1040C2 6006A1090 6006A1116 6006A1109 6006A1037C2 6006A1053C3 6006A1102 6006A1108 6006A1120 6006A1155 6006A1127 6006A1139 6006A1095C2 6006A1131 6006A1132 6006A1142 6006A1152 6006A1193 6006A1194 6006A1208 6006A1209 6006A1107 6006A1064C 6006A1068C 6006A1081C 6006A1011C2 6006A1104 6006A1101 6006A1087C 6006A1075C 6006A1035C2 6006A1057C2 6006A1044C2 6006A1024C2 6006A1059C3 6006A1083C3 6006A1119 6006A1124 6006A1128 6006A1071C2 6006A1089 6006A1084 6006A1042C2 6006A1078C2 6006A1082C2 6006A1027C2 6006A1010C2 6006A1125 6006A1147 6006A1025C2 6006A1077C 6006A1076C
- Quantity
- 78
- Classification
- Class II
Identifiers and details
- FDA event ID
- 99372
- Initiated
- Voluntary: Firm initiated
- Status
- Ongoing
- Firm location
- Pymble, Australia
Why it was recalled
The reason the FDA lists: “Due to an internal sensor issue, image displayed with eyepiece may appear tilted relative to the eyepiece housing”
Where it was sold
15 states: Arizona, California, Florida, Illinois, Iowa, Kansas, Kentucky, Nebraska, New York, Puerto Rico, Rhode Island, Texas, Virginia, Washington, Wisconsin. Distribution as the FDA records it: “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”
What to do
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Official notice: FDA Enforcement Report record (event 99372, openFDA) – the same recall numbers can be searched in the FDA Enforcement Report.
Other medical device recalls
| Date | Recall | Problem | Agency |
|---|---|---|---|
| Oct 7, 2026 |  Draeger recall: VentStar Resus NeoMedical devices · 1,063,643 units | Potential cracks in the hose, which could lead to leakage or the hose falling off. Most serious | FDA Class I |
| Oct 7, 2026 | Medline Industries recall: Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories and 1 more productMedical devices · 771,127 total | a fire hazard Most serious | FDA Class I |
| Oct 7, 2026 | Karl Storz Endoscopy recall: HOPKINS Telescope 30¿Medical devices · 6 eyepieces | Due to incorrect inside packaging label for eyepiece. Serious | FDA Class II |
| Oct 7, 2026 | Noxbox recall: NOxBOXi Nitric Oxide Delivery SystemMedical devices · 1,667 units | Potential for irregular oxygen readings due to a manufacturing issue affecting certain oxy… Serious | FDA Class II |
| Oct 7, 2026 | Siemens Healthcare Diagnostics recall: Atellica CH Revised C-Reactive ProteinMedical devices · 42940 units (3938 US, 39002 OUS) | The potential for falsely elevated results. Serious | FDA Class II |
| Oct 7, 2026 | Tandem Diabetes Care recall: T:slim Mobile ApplicationMedical devices · 177 | A beta (early-release) version of the iOS application, version 2.13 (TestFlight) had a sof… Serious | FDA Class II |
About this recall
Is Kico Knee Innovation Arvis Surgical Navigation System Gen 2 recalled?
Yes. Kico Knee Innovation Company recalled it on July 13, 2026; FDA published it August 26, 2026 (Class II). Only the lots, dates or models listed on this page are included.
Why was it recalled?
Due to an internal sensor issue, image displayed with eyepiece may appear tilted relative to the eyepiece housing
What should I do if I have it?
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Where was it sold?
In 15 states (Arizona, California, Florida, Illinois, Iowa, Kansas, Kentucky, Nebraska, New York, Puerto Rico, Rhode Island, Texas, Virginia, Washington, Wisconsin).
More recalls
Source: recall records published by the U.S. Food and Drug Administration (openFDA Enforcement Reports), the USDA Food Safety and Inspection Service, the Consumer Product Safety Commission and the National Highway Traffic Safety Administration, collected twice a day. Product names, lot codes, dates and model numbers are shown exactly as the agency lists them; the agency's notice is the authority. 77.today is not affiliated with any of these agencies.