Recall Z-0166-2020— Community Products, LLC

Name: FDA recall Z-0166-2020
Creator: U.S. Food and Drug Administration
Published: 2019-03-21

Class II · Terminated

Class II FDA medical device recall by Community Products, LLC, initiated 2019-03-21, terminated 2020-06-15. FDA's recall record names no specific 510(k) clearance for this event. Product: Rifton E-Pacer, SKU K660, powered lift device. Reason: A design change to the load-bearing quick release buckle renders the springs in the latch mechanism susceptible to fatigue failure after repeated use..

Recalling firm: Community Products, LLC
Classification: Class II
Status: Terminated
Initiated: 2019-03-21
Terminated: 2020-06-15
Firm location: Rifton, NY, United States

Product description

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.

Data sourced from openFDA. This site is unofficial and independent of the FDA.