# FDA recall Z-1138-2026

> **Community Products, LLC** · Class II · device recall initiated 2025-12-18.

## Product

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 variant includes smaller casters and lower base frame so that the legs fit underneath beds.

## 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

- **Recall number:** Z-1138-2026
- **Recalling firm:** Community Products, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-12-18
- **Report date:** 2026-01-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Rifton, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1138-2026

## Citation

> AI Analytics. FDA recall Z-1138-2026. Retrieved 2026-07-29 from https://api.ai-analytics.org/recall/Z-1138-2026. Source: US FDA. Licensed CC0.

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