FDA recall, , Moderate risk
Community Products Rifton Equipment TRAM and E-Pacer Powered Lifts
The TRAM and E-Pacer have a potential for fraying on the body support strap.
Summary by Recall Canary from the FDA notice
What happened
Community Products, LLC of Rifton, New York began a recall on December 18, 2025, for Rifton Equipment products including the Low Base TRAM (K320), E-Pacer (K660), and TRAM (K310) due to a potential for fraying on the body support strap. The recall was added to the FDA's Enforcement Report and classified on January 22, 2026, with distribution worldwide, including the US and countries such as UAE, Australia, Canada, EU, Israel, Hong Kong, Japan, Korea, New Zealand, Russia, Saudi Arabia, and UK.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
3 products
Compare these details with yours, then check the recall notice to see which units are recalled.
Rifton Equipment, Low Base TRAM. Model/Catalog Number: K320. The TRAM
Rifton Equipment, E-Pacer. Model/Catalog Number: K660. The E-Pacer
Rifton Equipment, TRAM. Model/Catalog Number: K310. The TRAM
Recall details
- Company began the recall
- Sold in
Worldwide distribution - US Nationwide and the countries of UAE, Australia, Canada, EU, Israel, Hong Kong, Japan, Korea, New Zealand, Russia, Saudi Arabia, and UK.
- Company
- Community Products, LLCRifton, New York
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98140
- Recall numbers
- Z-1137-2026 to Z-1139-2026
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Listed on Recall Canary
