HIGHFDA DEVICE

Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the following components: IN-10500, Impactor V-Block Assembly; IN-10600 , Tracker B; IN-16400, Tracker A; IN-16100, Tracker C;...

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 Knee InnovationHealth & Personal CareMedical DevicesAll Lots/serial NumbersUDI: IN-28000: 00810180350020IN-10500: (01)00810180350686

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
April 23, 2026
Status
ACTIVE

Quick Facts at a Glance

Recall Date
April 23, 2026
Hazard Level
HIGH
Brand
Kico Knee Innovation
Geographic Scope
1 states

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Kico Knee Innovation
Model numbers
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
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    April 23, 2026

  2. Reported by FDA DEVICE

    June 10, 2026

  3. RecallRadar source check

    June 16, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

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.

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Kico Knee Innovation Company or your healthcare provider for instructions. Notification method: Letter

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Full Description

Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the following components: IN-10500, Impactor V-Block Assembly; IN-10600 , Tracker B; IN-16400, Tracker A; IN-16100, Tracker C; IN-28050, Tracker E. Reason: 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.. Classification: Class II. Quantity: 69 units. 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.

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: How to Get Refunds and Replacements

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Product Classification

Product Details

Model Numbers
All Lots/serial Numbers
UDI: IN-28000: 00810180350020
IN-10500: (01)00810180350686
IN-10600 (01)00810180350693
IN-16400:(01)00810180350525
+2 more
Affected States
ALL
Report Date
June 10, 2026
Recall Status
ACTIVE