PlainRecalls
FDA Devices Moderate Class II Ongoing

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.

Reported: January 28, 2026 Initiated: December 18, 2025 #Z-1139-2026

Product Description

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.

Reason for Recall

Potential for fraying on the body support strap.

Details

Recalling Firm
Community Products, LLC
Units Affected
470 units
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.
Location
Rifton, NY

Frequently Asked Questions

What product was recalled?
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.. Recalled by Community Products, LLC. Units affected: 470 units.
Why was this product recalled?
Potential for fraying on the body support strap.
Which agency issued this recall?
This recall was issued by the FDA Devices on January 28, 2026. Severity: Moderate. Recall number: Z-1139-2026.