# FDA recall Z-0165-2020

> **Community Products, LLC** · Class II · device recall initiated 2019-03-21.

## Product

Rifton TRAM Low Base, SKU K320, powered lift device

## Reason for recall

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, New Zealand, Israel, Colombia,  Russia

## Key facts

- **Recall number:** Z-0165-2020
- **Recalling firm:** Community Products, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-03-21
- **Report date:** 2019-10-30
- **Termination date:** 2020-06-15

- **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-0165-2020

## Citation

> AI Analytics. FDA recall Z-0165-2020. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/Z-0165-2020. Source: US FDA. Licensed CC0.

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