PlainRecalls
FDA Devices Moderate Class II Terminated

Rifton TRAM Low Base, SKU K320, powered lift device

Reported: October 30, 2019 Initiated: March 21, 2019 #Z-0165-2020

Product Description

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.

Details

Recalling Firm
Community Products, LLC
Units Affected
1079
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
Location
Rifton, NY

Frequently Asked Questions

What product was recalled?
Rifton TRAM Low Base, SKU K320, powered lift device. Recalled by Community Products, LLC. Units affected: 1079.
Why was this product 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.
Which agency issued this recall?
This recall was issued by the FDA Devices on October 30, 2019. Severity: Moderate. Recall number: Z-0165-2020.