Arvis Hip & Knee 3.0 Instrument Set
Kico recalls Arvis Hip & Knee 3.0 Instrument Set over magnet face wear/corrosion.
Stop using the affected instrument set and contact Kico Knee Innovation Company for instructions on returning the device 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 and/or corrosion on the exposed magnet face, which could affect surgical accuracy. The affected components are IN-10500, IN-10600, IN-16400, IN-16100, and IN-28050.
Is mine affected?
Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.
Lot code: All Lots/serial Numbers
| Product | Recall # | UDI-DI |
|---|---|---|
| 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 | Z-2292-2026 | 00810180350020, 00810180350686, 00810180350693, 00810180350525, 00810180350563, 00810180350051 |
| 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 | Z-2293-2026 | 00810180350020, 00810180350686, 00810180350693, 00810180350525, 00810180350563 |
Where it was sold
Distributed nationwide.
Timeline
- Firm initiated recall
- Publicly announced
- Listed on Recall Canary
- Summary updated
Official source
Other recent recalls from Kico Knee Innovation Company
Editorial summary by Recall Canary · summary updated 2026-09-08 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification