FDA Recall Open, Classified

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.

Recall: Z-1139-2026 · Initiated December 18, 2025

Recall

Recall Number
Z-1139-2026
Event Number
98140
Firm
Community Products, LLC
FEI Number
1319061
Product Code
FSA
Status
Open, Classified
Root Cause
Process change control
Initiated
December 18, 2025
Posted
January 22, 2026
Address
2032 Route 213, Rifton, NY, 12471

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

Potential for fraying on the body support strap.

Action

Community Products notified consignees via email on about 12/18/2025. Consignees were instructed to notify all customers, if further distributed, of the recall, inspect all affected devices for visible fraying, and cease use if any is observed. Consignees were requested to provide contact information for the individual responsible for performing the replacement. If devices were further distributed, consignees were advised to manage all customer outreach, inspection and replacement. The other option was to provide Community Products with customer contact information, and Rifton will manage the process. Lastly, consignees were requested to confirm receipt of the notification.

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.

Quantity

470 units