Community Products, LLC recalls Rifton E-Pacer, SKU K660, powered lift device

Recall date

March 21, 2019

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-0166-2020

FDA classification

Class II

Brand / firm

Community Products, LLC

Sold / distributed

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 Zea…

Why it was recalled

A design change to the load-bearing quick release buckle renders the springs in the latch mechanism susceptible to fatigue failure after repeated use.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Rifton E-Pacer, SKU K660, powered lift device