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.
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.
Kico is recalling Arvis Hip & Knee 3.0 Instrument Sets with serial numbers starting with 00810180350020 due to possible early wear and corrosion on magnet faces. This could lead to reduced performance or failure during use, especially in medical procedures.
The exposed magnet faces in the V-Block Assembly and Trackers A, B, C, and E may corrode or wear prematurely. This could cause the instruments to malfunction during surgery, potentially affecting precision and safety.
Medical professionals using the Arvis Hip & Knee 3.0 Instrument Set for surgical procedures are most at risk. The recall affects specific models and serial numbers produced by Kico Knee Innovation Company.
Check if your Arvis Hip & Knee 3.0 Instrument Set has a serial number starting with 00810180350020 or includes specific components like IN-10500, IN-10600, IN-16400, IN-16100, or IN-28050. The recall covers all lots and serial numbers listed in the product description.
Inspect the magnet faces of the V-Block Assembly and Trackers A, B, C, and E for corrosion or early wear.
Yes, if your Arvis Hip & Knee 3.0 Instrument Set has a serial number starting with 00810180350020 or includes the specified components, it is affected.
Check the serial number on your instrument; affected units have serial numbers starting with 00810180350020 or include specific components like IN-10500, IN-10600, IN-16400, IN-16100, or IN-28050.
Inspect the magnet faces for signs of corrosion or wear. If you find issues, contact Kico for further guidance.
We’ve drafted a message you can send Kico to request your refund or repair — edit it as you like.
Subject: Recall Z-2292-2026 — Kico Kico Hello, I own a Kico that is covered by recall Z-2292-2026 from Kico. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
