FDA recall Z-1139-2026

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 for recall

Potential for fraying on the body support strap.

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.

Key facts

Status

Ongoing

Initiation date

2025-12-18

Report date

2026-01-28

Voluntary/Mandated

Voluntary: Firm initiated

Location

Rifton, NY, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1139-2026