Kico Knee Innovation Company recalls
Every recall we track for Kico Knee Innovation Company — 4 in all, from 2025–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
4 recalls since 2017.
All FDA recall records for Kico Knee Innovation Company since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 1 | 0 | 1 |
| 2026 (to date) | 0 | 0 | 3 | 0 | 3 |
What to do if you have a recalled Kico Knee Innovation Company product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Kico Knee Innovation Company recalls
3 shown- Lower riskMedical device
Kico Knee Innovation Company recalls Brand Name: Kico Knee Innovation Product Name: ARVIS SURGICAL NAVIGATION SYSTEM GEN 2 Model/Catalog Number: IN-29200
Kico recalls ARVIS Surgical Navigation System Gen 2 (model IN-29200) due to potential image tilt in eyepiece. This may affect surgical alignment accuracy during procedures like knee or hip replacements.
KicoJul 13, 2026 - Lower riskMedical device
Kico Knee Innovation Company recalls Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the following components: IN-10500, Impactor
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.
KicoApr 23, 2026 - Lower riskMedical device
Kico Knee Innovation Company recalls Brand Name: ARVIS Product Name: ARVIS" Shoulder Model/Catalog Number: IN-27300, Arvis Surgical Planning Software
Kico Knee Innovation Company recalls ARVIS Shoulder surgical planning software version V2025.1.2 due to potential implant malalignment or reduced range of motion. Affected users should contact for remedy.
ARVISSep 19, 2025
Kico Knee Innovation Company recall questions
How many recalls has Kico Knee Innovation Company had?
4 recalls from Kico Knee Innovation Company are on record with U.S. safety agencies, from 2025–2026.
What is the most recent Kico Knee Innovation Company recall?
Kico Knee Innovation Company recalls Brand Name: Kico Knee Innovation Product Name: ARVIS SURGICAL NAVIGATION SYSTEM GEN 2 Model/Catalog Number: IN-29200, dated Jul 13, 2026. Every Kico Knee Innovation Company recall is listed on this page, newest first.
What should I do if I have a recalled Kico Knee Innovation Company product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Kico Knee Innovation Company recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.