Reported Jun 10, 2026 · Ongoing
Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000 containing one of the following components: IN-10500, Impactor…
Kico Knee Innovation Company
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Kico Knee Innovation Company · Suite 3, Building 1, 20 Bridge St · Pymble · N/A
Is this the product you have?
- Arvis Hip & Knee 3.0 Instrument Set
- REFIN-28000 containing
- one of the following componentsIN-10500, Impactor V-Block Assembly; IN-10600 , Tracker B; IN-16400, Tracker A; IN-16100, Tracker C; IN-28050, Tracker E
- Lot codes and dates
- All Lots/serial Numbers
- UDIIN-28000: 00810180350020
- IN-10500
(01)00810180350686IN-10600 (01)00810180350693
- IN-16400(01)00810180350525
- IN-16100(01)00810180350563
- IN-2805000810180350051
- Amount recalled
- 69 units
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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