Recall Z-0557-2013— ThyssenKrupp Access Corp

Name: FDA recall Z-0557-2013
Creator: U.S. Food and Drug Administration
Published: 2012-08-06

Class II · Terminated

Class II FDA medical device recall by ThyssenKrupp Access Corp, initiated 2012-08-06, terminated 2014-01-29. It names one FDA 510(k) clearance: K121560. Product: ThyssenKrupp Accessibility LEVANT Stairlift. Intended to mechanically transport one mobility impaired person in a fold-down seat up and down straight stairs, indoors and outdoors.. Reason: The seat could break as a result of damage resulting from a seat belt being trapped underneath the foldable part of the seat when the seat belt is not buckled..

Recalling firm: ThyssenKrupp Access Corp
Classification: Class II
Status: Terminated
Initiated: 2012-08-06
Terminated: 2014-01-29
Firm location: Grandview, MO, United States

510(k) clearances named in this recall

1 on FDA's record

K121560 — LEVANT, HOMEGLIDEThyssenkrupp Accessibility B.V.·cleared 2012-11-01

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

ThyssenKrupp Accessibility LEVANT Stairlift. Intended to mechanically transport one mobility impaired person in a fold-down seat up and down straight stairs, indoors and outdoors.

Reason for recall

The seat could break as a result of damage resulting from a seat belt being trapped underneath the foldable part of the seat when the seat belt is not buckled.

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