Kico Knee Innovation Company recalls Brand Name: Kico Knee Innovation Product Name: ARVIS SURGICAL NAVIGATION SYSTEM GEN 2 Model/Catalog Number: IN-29200 Software…
Due to an internal sensor issue, image displayed with eyepiece may appear tilted relative to the eyepiece housing
Read the official notice →- Date
- 2026-08-26
- Country
- United States
- Brand
- Kico Knee Innovation
- Product
- Brand Name: Kico Knee Innovation Product Name: ARVIS SURGICAL NAVIGATION SYSTEM GEN 2 Model/Catalog Number: IN-29200 Software Version:…
- Classification
- Class II
- Units
- Consignee Consignee Number Region Device Quantity RFK MEDICAL CE102 RICHMOND…
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Kico Knee Innovation recalls
- 2026-06-10
USKico Knee Innovation Company recalls Arvis Hip & Knee 2.0 Instrument Set, REF: IN-21200 containing one of the following components: IN-10500, Impactor V-Block Assembly;…
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.
FDA · DeviceKico Knee Innovation CompanyWorldwide - US Nationwide distribution in the states of MS, CA, IA, IN, MI,…Official notice →- US
Kico Knee Innovation Company recalls Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the following components: IN-10500, Impactor V-Block Assembly;…
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.
FDA · DeviceKico Knee Innovation CompanyWorldwide - US Nationwide distribution in the states of MS, CA, IA, IN, MI,…Official notice → - 2025-10-22
- US
Kico Knee Innovation Company recalls Brand Name: ARVIS Product Name: ARVIS" Shoulder Model/Catalog Number: IN-27300, Arvis Surgical Planning Software Software Version:…
Complaint identified issue with AI surgical planning software that may result in implant malalignment and/or decrease range of motion.
FDA · DeviceKico Knee Innovation CompanyUS Nationwide distribution in the states of IN, MN, MO, OH, FL, IL, RI, KY,…Official notice →
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