Moller Vital: Medical Device Recall in 2013 - (Recall #: Z-1343-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Molift Smart 150

Product Classification:

Class II

Date Initiated: February 15, 2013

Date Posted: May 29, 2013

Recall Number: Z-1343-2013

Event ID: 64512

Reason for Recall:

The leg spreading mechanism will fail to hoist and collapse if assemble incorrectly by the user.

Status: Terminated

Product Quantity: Subject to recall 1,460 units; US: 175 units; Foreign: 1,285 units

Code Information:

Art #: 0920008; Serial Number range 20941 to 27299.

Distribution Pattern:

US Nationwide Distribution: CA, FL, GA, ID, IL, KY, MA, ME, MI, MN, NC, NH, NJ, NM, NV, NY, OH, OK, PA, TN, TX, VT, WA and Hawaii. Foreign Distribution:: Australia, Austria; Belgium, Denmark, Finland, France, Germany, Iceland, Israel, Italy, Japan, Netherlands, New Zealand, Norway, Spain, Sverige, Switzerland, United Kingdom.

Voluntary or Mandated:

Voluntary: Firm initiated