Medical device recalls Moderate risk

Community Products, LLC recalls Rifton Equipment, E-Pacer. Model/Catalog Number: K660. The E-Pacer is a gait training device with power height adjustme…

Recall date
December 18, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1139-2026
FDA classification
Class II
Brand / firm
Community Products, LLC
Sold / distributed
Worldwide distribution - US Nationwide and the countries of UAE, Australia, Canada, EU, Israel, Hong Kong, Japan, Korea, New Zealand, Russia, Saudi Arabia, and UK.

Why it was recalled

Potential for fraying on the body support strap.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What 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.

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