Recall database

Ankle Arthroplasty Implantation System recalls

Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.

Showing 1–1 of 1 recalls

Class IIOngoingZ-3178-2026

Restor3d Inc. recalls Kinos Axiom Total Ankle System with Axiom PSR

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, imp…

Ankle Arthroplasty Implantation System
Labeling Change Control

restor3d Inc.NCSep 23, 2026