FDA recall, , Moderate risk
Arvis Hip & Knee 2.0 and 3.0 Instrument Set
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.
Summary by Recall Canary from the FDA notice
What happened
Kico Knee Innovation Company of Pymble, Australia, began a recall on April 23, 2026, for the Arvis Hip & Knee 3.0 Instrument Set and the Arvis Hip & Knee 2.0 Instrument Set because the Impactor V-Block Assembly and Trackers A, B, C and E may exhibit signs of early wear and/or corrosion on the exposed magnet face.
The FDA added the recall to its Enforcement Report on June 2, 2026, and the products were distributed nationwide in the United States and internationally in Australia, France, Germany and Italy.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is your set affected?
2 products
Affected if its UDI-DI is listed.
A UDI-DI is the device identifier printed with the barcode on the device label.
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
Reason: 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.
- UDI-DI
- 00810180350020
- 00810180350686
- 00810180350693
- 00810180350525
- 00810180350563
- 00810180350051
- Lot code
- All Lots/serial Numbers
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
Reason: The Impactor V-Block Assembly and Trackers A, B, C and E may exhibit signs of early wear and/or corrosion on the exposed magnet face.
- UDI-DI
- 00810180350020
- 00810180350686
- 00810180350693
- 00810180350525
- 00810180350563
- Lot code
- All Lots/serial Numbers
Recall details
- Company began the recall
- Sold in
Worldwide - US Nationwide distribution in the states of Mississippi, California, Iowa, Indiana, Michigan, Colorado, Montana, Florida, Illinois, New York, Alabama, Wisconsin, Nebraska, Arizona, Minnesota, Vermont, New Hampshire, Maryland, Rhode Island, Massachusetts, New Jersey, Pennsylvania, Kansas, Washington, Idaho, Oregon, Tennessee, Virginia, PR and the countries of Australia, France, Germany, Italy.
- Company
- Kico Knee Innovation CompanyPymble, Australia
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98804
- Recall numbers
- Z-2292-2026 to Z-2293-2026
All recalls from Kico Knee Innovation Company
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated