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Community Products, LLC recalls Rifton E-Pacer, SKU K660, powered lift device
Recalled October 30, 2019 · FDA recall Z-0166-2020 · Community Products
Hazard
A design change to the load-bearing quick release buckle renders the springs in the latch mechanism susceptible to fatigue failure after repeated use. · FDA Class II
Units
167
Sold at
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
Description
A design change to the load-bearing quick release buckle renders the springs in the latch mechanism susceptible to fatigue failure after repeated use.
Product
Rifton E-Pacer, SKU K660, powered lift device
Manufacturer(s)
Community Products, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →