ClearanceBrief
Recall Z-1343-2013 ยท FSA Lift, Patient, Non-Ac-Powered

Moller Vital

Molift Smart 150

DateMay 21, 2013 (initiated Feb 15, 2013)
StatusTerminated
ReasonThe leg spreading mechanism will fail to hoist and collapse if assemble incorrectly by the user.
Root causeEmployee error
ActionMolift Group AS issued a Field Safety Notice letter to all affected customers. The letter identified the affected products, problem and actions to be taken to the Smart hoists that are already in use. Customers were instructed to make sure that all affected customers receive this information and encorage to increase attention until the affected product has been upgraded. For questions contact your local Molift representative or Customer Service at: groupsales@molift.com.
QuantitySubject to recall 1,460 units; US: 175 units; Foreign: 1,285 units
DistributionUS 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,
FDA recordOpen on fda.gov

510(k) clearances named in this recall

This recall record lists no 510(k) number.