Arvis Hip & Knee 2 — Class II medical device recall Z-2293-2026
Ongoing recall by Kico Knee Innovation Company, reported 2026-06-10, distributed nationwide. The Impactor V-Block Assembly and Trackers A, B, C and E may exhibit signs of early wear and/or corrosion on t
| Recall number | Z-2293-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Kico Knee Innovation Company, Pymble, Australia |
| Recall initiated | 2026-04-23 |
| Classified | 2026-06-02 |
| Reported by FDA | 2026-06-10 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, DE, FR, IT |
| Quantity | 124 kits |
| UPC / GTIN / UDI-DI | 00810180350020, 00810180350525, 00810180350563, 00810180350686, 00810180350693 |
| Model numbers | IN-21200 |
Product
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 for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2293-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.