Arvis Hip & Knee 3.0 Instrument Set
Kico Knee recalls Arvis Hip & Knee 3.0 Instrument Set due to wear/corrosion on magnet face of V-Block and Trackers.
Stop using the affected instrument set immediately. Contact Kico Knee Innovation Company for instructions on returning the components for inspection and replacement.
Why it was recalled
Kico Knee Innovation Company is recalling the Arvis Hip & Knee 3.0 Instrument Set (REF: IN-28000) because the V-Block Assembly and Trackers A, B, C, and E may exhibit early wear or corrosion on the exposed magnet face, which could affect surgical accuracy.
Is mine affected?
Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.
| Product | UPC | Recall # |
|---|---|---|
| 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 | 00810180350020, 00810180350686, 00810180350693, 00810180350525, 00810180350563, 00810180350051 | Z-2292-2026 |
| 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 | 00810180350020, 00810180350686, 00810180350693, 00810180350525, 00810180350563 | Z-2293-2026 |
Where it was sold
Distributed nationwide.
Official source
Editorial summary by Recall Canary · last updated 2026-07-28 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification