Rifton, NY, United States

Community Products, LLC recalls

2 recalls recorded since 2018, most recently on 18 December 2025. 1 is listed as ongoing. Status and classification are as published by the FDA.

Recalls2

Ongoing (FDA)1

Terminated or completed1

Class I (FDA)0

Recall started: 18 December 2025
Reason: 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.
Initiated: Voluntary: Firm initiated
Recall numbers: Z-1137-2026, Z-1139-2026, Z-1138-2026

Rifton Equipment, TRAM. Model/Catalog Number: K310. The TRAM is a powered lift device for transferring clients in a seated position or assisting in a sit-to-stand transfer and gait training.
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.
Rifton Equipment, Low Base TRAM. Model/Catalog Number: K320. The TRAM is a powered lift device for transferring clients in a seated position or assisting in a sit-to-stand transfer and gait training. The low base vari

Recall started: 21 March 2019
Terminated: 15 June 2020
Reason: A design change to the load-bearing quick release buckle renders the springs in the latch mechanism susceptible to fatigue failure after repeated use.
Distribution: The products were distributed US nationwide. The products were distributed to the following foreign countries: Foreign Countries: Worldwide, including Canada, United Kingdom, Germany, Japan, Singapore, South Korea, United Arab Emirates, Taiwan, Denmark, Italy, Hong Kong, Ireland, Australia, N
Initiated: Voluntary: Firm initiated
Recall numbers: Z-0164-2020, Z-0165-2020, Z-0166-2020

A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.