FDAClass IIMay 29, 2013

Molift Smart 150 recall

Molift Smart 150

Why was Molift Smart 150 recalled?

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

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

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

Product
Molift Smart 150
Recalling firm
Moller Vital
Quantity
Subject to recall 1,460 units; US: 175 units; Foreign: 1,285 units
Distribution
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.
Recall date
May 29, 2013
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls