FDA recall Z-0166-2020

Product

Rifton E-Pacer, SKU K660, 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

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

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0166-2020