Kico Knee Innovation recalls Arvis Hip & Knee 2.0 Instrument Set with possible early wear and corrosion on magnet faces. Affected units include specific model numbers and serial ranges. Consumers should check their instruments for signs of wear.
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.
Kico Knee Innovation is recalling Arvis Hip & Knee 2.0 Instrument Sets that may have early wear or corrosion on the magnet faces. This could lead to reduced performance or failure during use, especially in medical procedures.
The magnet faces on the Impactor V-Block Assembly and Trackers A, B, C, and E may corrode or wear early, potentially causing the device to malfunction during surgery. This could lead to reduced precision or failure in critical medical procedures.
Medical professionals using the Arvis Hip & Knee 2.0 Instrument Set for surgical procedures are most at risk. Patients receiving these instruments during surgery may also be affected if the device malfunctions.
Check for the model number IN-21200 on the Arvis Hip & Knee 2.0 Instrument Set. Affected units include specific serial numbers and lots listed in the recall notice.
Inspect the magnet faces for signs of corrosion or wear on the Impactor V-Block Assembly and Trackers A, B, C, and E.
The recall indicates possible early wear or corrosion on magnet faces, which could affect device performance during surgery. However, the hazard is not described as causing serious injury in normal use.
Check the model number and serial numbers listed in the recall notice: IN-21200 with specific serial ranges like 00810180350020, 00810180350686, etc.
The recall does not specify a remedy, so you should check for signs of wear or corrosion and contact the manufacturer for further guidance.
We’ve drafted a message you can send Kico Knee Innovation to request your refund or repair — edit it as you like.
Subject: Recall Z-2293-2026 — Kico Knee Innovation Kico Knee Innovation Hello, I own a Kico Knee Innovation that is covered by recall Z-2293-2026 from Kico Knee Innovation. 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.
