Arvis Hip & Knee 3.0 Instrument Set Recall
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Kico Knee Innovation Company is recalling 69 units of the Arvis Hip & Knee 3.0 Instrument Set due to potential early wear and corrosion on components.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on July 10, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, medical-devices.
What Happened
Kico Knee Innovation Company initiated a voluntary recall of the Arvis Hip & Knee 3.0 Instrument Set because 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.
Which Products Are Affected
The recall affects 69 units of Arvis Hip & Knee 3.0 Instrument Set, REF: IN-28000, containing components IN-10500 (Impactor V-Block Assembly), IN-10600 (Tracker B), IN-16400 (Tracker A), IN-16100 (Tracker C), and IN-28050 (Tracker E). All lots/serial numbers are included. UDI codes: IN-28000: 00810180350020; IN-10500: (01)00810180350686; IN-10600: (01)00810180350693; IN-16400: (01)00810180350525; IN-16100: (01)00810180350563; IN-28050: 00810180350051. Distribution includes US nationwide in 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 countries Australia, France, Germany, Italy. Recall number Z-2292-2026. Classification: Class II.
What You Should Do
Consumers should follow instructions provided in the firm's notification letter regarding the affected devices.
Why This Matters
The recall involves medical devices distributed across the United States and internationally that may experience component degradation.
Source
FDA recall Z-2292-2026 (event ID 98804).
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,338 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to July 10, 2026.
Frequently Asked Questions
Common questions about this FDA recall.