Kico Knee Innovation Company recalls Arvis Hip & Knee 2.0 Instrument Set

Recalling company

Kico Knee Innovation Company

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

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.

Classification

Class II – may cause temporary or medically reversible health consequences

Recall date

Apr 23, 2026

Reported

Jun 10, 2026

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.

Status

Ongoing

Quantity

124 kits

Lot / codes

All Lots/serial Numbers; UDI: IN-28000: 00810180350020; IN-10500: (01)00810180350686; IN-10600 (01)00810180350693; IN-16400:(01)00810180350525; IN-16100: (01)00810180350563;

Company location

Pymble

Recall type

Voluntary: Firm initiated

Recall number

Z-2293-2026

Agency

U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number Z-2293-2026 in the FDA Enforcement Report. Also see FDA recall press releases.