Community Products, LLC: Device Recall
Recall #Z-1139-2026 · 12/18/2025
Class II: Risk
Recall Details
- Recall Number
- Z-1139-2026
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Community Products, LLC
- Status
- Ongoing
- Date Initiated
- 12/18/2025
- Location
- Rifton, NY, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 470 units
Reason for Recall
Potential for fraying on the body support strap.
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.
Distribution Pattern
Worldwide distribution - US Nationwide and the countries of UAE, Australia, Canada, EU, Israel, Hong Kong, Japan, Korea, New Zealand, Russia, Saudi Arabia, and UK.
Other Recalls by Community Products, LLC
- Class II: Risk 12/18/2025
- Class II: Risk 12/18/2025
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.