---
title: "Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the foll... — FDA record Z-2292-2026 | Is It on Recall"
description: "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."
url: https://isitonrecall.com/recall/fda-device-z-2292-2026-arvis-hip-knee-3-0-instrument-set-ref-in-28000-containing-one-of-the-following-components-in-10500-i/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the following components: IN-10500, Impactor V-B... — FDA record Z-2292-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Apr 23, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: 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.
- **Classification**: Class II
- **Recalling firm**: Kico Knee Innovation Company
- **Quantity**: 69 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2292-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2292-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | All Lots/serial Numbers; UDI: IN-28000: 00810180350020; IN-10500: (01)00810180350686; IN-10600 (01)00810180350693; IN-16400:(01)00810180350525; IN-16100: (01)00810180350563; IN-28050: 00810180350051 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Worldwide - US Nationwide distribution in the states of MS, CA, IA, IN, MI, CO, MT, FL, IL, NY, AL, WI, NE, AZ, MN, VT, NH, MD, RI, MA, NJ, PA, KS, WA, ID, OR, TN, VA, PR and the countries of Australia, France, Germany, Italy.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Jun 10, 2026
- **Recall initiation date**: Apr 23, 2026
- **Center classification date**: Jun 2, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2292-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Kico Knee Innovation Company records](https://isitonrecall.com/brand/kico-knee-innovation-company/)
