- Recalling firm
- Kico Knee Innovation Company
- Reason for recall
- 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.
- Affected products (lot / model / serial)
- 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
- Units affected
- 69 units
- Distribution pattern
- 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.
- Firm location
- Pymble, Australia
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2292-2026
- Recall initiated
- April 23, 2026
- FDA classification date
- June 2, 2026
- FDA report date
- June 10, 2026
- FDA event ID
- 98804
- Last updated on HTM Vibe
- July 23, 2026