FDAJuly 27, 2026
restor3d Kinos Axiom Total Ankle System Recall Over Incorrect Cutting Guides
FDA published this notice on July 27, 2026 for United States.
This notice is kept at its address for anyone who saved the link. AreaZine no longer holds the agency's full record for it, so the page shows what AreaZine recorded and links to the agency's own page, the one to read.
What AreaZine recorded
- Agency
- FDA
- Place
- United States
- Date
- July 27, 2026
- Recall class
- Class II
- Reason given by the agency
- Ankle implantation systems were packaged with incorrect patient-specific cutting guides, which may result in: delayed surgery, the need to use standard instrumentation, reduced fixation or poor alignment of implants, implant loosening/migration, or need for revision surgery.
- Distribution
- US Nationwide distribution in the states of FL, CO.
- Official source
- the notice at its source
Official warnings by state, with every type counted since 2008Search notices, places and declaration numbers
Source: FDA.