Recall Z-1139-2026— Community Products, LLC
Class II · Ongoing
Class II FDA medical device recall by Community Products, LLC, initiated 2025-12-18. FDA's recall record names no specific 510(k) clearance for this event. Product: 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: Potential for fraying on the body support strap..
- Recalling firm
- Community Products, LLC
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2025-12-18
- Firm location
- Rifton, NY, United States
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.