Lower riskMedical device recall · FDA · Published April 23, 2026
Kico Arvis Hip & Knee 3.0 Instrument Set Recall: Early Wear/Corrosion Risk
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.
The V-Block Assembly and Trackers A, B, C and E may exhibit signs of early wear and/or corrosion on the exposed magnet face.
Take action
Contact the company
📍Recalling firmKico Knee Innovation CompanySuite 3, Building 1, 20 Bridge St · Pymble, Australia
✎ GovInfoNow plain-language explainer
Kico is recalling Arvis Hip & Knee 3.0 Instrument Sets with serial numbers starting with 00810180350020 due to possible early wear and corrosion on magnet faces. This could lead to reduced performance or failure during use, especially in medical procedures. Read more at govinfonow.com/recall/49392-kico-arvis-hip-knee-3-0-instrument-set-recall-early.
“Kico Arvis Hip & Knee 3.0 Instrument Set Recall: Early Wear/Corrosion Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/49392-kico-arvis-hip-knee-3-0-instrument-set-recall-early. Based on FDA recall #Z-2292-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2292-2026%22&limit=1).
Kico Knee Innovation Company recalled Arvis Hip & Knee 3.0 Instrument Sets containing specific components due to potential early wear and corrosion on exposed magnet faces, the FDA said April 23, 2026.
How to tell if you have it
Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000
IN-10500, Impactor
IN-10600, Tracker B
IN-16400, Tracker A
IN-16100, Tracker C
IN-28050, Tracker E
The hazard
The V-Block Assembly and Trackers A, B, C and E may exhibit signs of early wear and/or corrosion on the exposed magnet face.
Context
GovInfoNow's records show Kico Knee Innovation Company has two other recalls since September 19, 2025, including a July 13, 2026 recall for ARVIS Surgical Navigation System Gen 2 and a September 19, 2025 recall for ARVIS Shoulder Surgical Software V2025.1.2. Other recent recalls of similar products include Codman CereLink ICP Sensor Basic Kit Recall (December 12, 2025), Howmedica Osteonics cobalt chrome elbow implants recall (July 30, 2026) and Howmedica SCORPIO C-DOME/PATELLA Implants Recall (July 30, 2026).
How to tell if you have this one
Check if your Arvis Hip & Knee 3.0 Instrument Set has a serial number starting with 00810180350020 or includes specific components like IN-10500, IN-10600, IN-16400, IN-16100, or IN-28050. The recall covers all lots and serial numbers listed in the product description.
Brand
Kico
Product
Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the following components: IN-10500, Impactor
Category
Medical device
FDA recall event · 2 products
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Ongoing
Distribution
Worldwide - US Nationwide distribution in the states of MS, CA, IA, IN, MI, CO, MT, FL, IL, NY, AL, WI, NE, AZ, MN, VT, NH, MD, RI, MA, NJ, PA, KS, WA, ID, OR, TN, VA, PR and the countries of Australia, France, Germany, Italy.
Recall number
Product, codes & lots
Quantity
Z-2292-2026
Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the following components: IN-10500, Impactor V-Block Assembly; IN-10600 , Tracker B; IN-16400, Tracker A; IN-16100, Tracker C; IN-28050, Tracker E; All Lots/serial Numbers; UDI: IN-28000: 00810180350020; IN-10500: (01)00810180350686; IN-10600 (01)00810180350693; IN-16400:(01)00810180350525; IN-16100: (01)00810180350563; IN-28050: 00810180350051
69 units
Z-2293-2026
Arvis Hip & Knee 2.0 Instrument Set, REF: IN-21200 containing one of the following components: IN-10500, Impactor V-Block Assembly; IN-10600 , Tracker B; IN-16400, Tracker A; IN-16100, Tracker C; All Lots/serial Numbers; UDI: IN-28000: 00810180350020; IN-10500: (01)00810180350686; IN-10600 (01)00810180350693; IN-16400:(01)00810180350525; IN-16100: (01)00810180350563;
124 kits
Based on the official FDA remedy
What to do — step by step
Check for Signs of Wear
Inspect the magnet faces of the V-Block Assembly and Trackers A, B, C, and E for corrosion or early wear.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 28 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA distribution: “Worldwide - US Nationwide distribution in the states of MS, CA, IA, IN, MI, CO, MT, FL, IL, NY, AL, WI, NE, AZ, MN, VT, NH, MD, RI, MA, NJ, PA, KS, WA, ID, OR, TN, VA, PR and the countries of Australia, France, Germany, Italy.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Alabama, Arizona, California, Colorado, Florida, Idaho, Illinois, Indiana, Iowa, Kansas, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Montana, Nebraska, New Hampshire, New Jersey, New York, Oregon, Pennsylvania, Puerto Rico, Rhode Island, Tennessee, Vermont, Virginia, Washington, Wisconsin.
Recall timeline
FDA published this recall 48 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-2292-2026 (April 23, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2292-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.