Class II

Medical Device Recall: Rifton Equipment, E-Pacer. Model/Catalog Number: K660. The E-Pacer is a gait training device with power height adjustment that facilitates the sit-to-stand motion.

Community Products, LLC · December 18, 2025

Reason for Recall

Potential for fraying on the body support strap.

Distribution

Worldwide distribution - US Nationwide and the countries of UAE, Australia, Canada, EU, Israel, Hong Kong, Japan, Korea, New Zealand, Russia, Saudi Arabia, and UK.

States Affected

NATIONWIDE

Quantity Affected

470 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1139-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.