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Terminated

Molift Smart 150

FDA Recall Z-1342-2013 · Posted 2013-05-21

Recalling FirmMoller Vital
Recall StatusTerminated
Product CodeFSA
Date Initiated2013-02-15
Date Terminated2014-07-11
Product Quantity7,555 units subject to review; US: 1,280 units - Foreign: 6,275 units

Reason for Recall

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

Firm Action

Molift 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: [email protected].

Root Cause

Employee error

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.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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