Z-1342-2013 Class II Terminated
FDA device recall Z-1342-2013 was initiated by Moller Vital on February 15, 2013 and is designated Class II. Reason for recall: The leg spreading mechanism will fail to hoist and collapse if assemble incorrectly by the user. The recall status is terminated (terminated July 11, 2014). Affected quantity: 7,555 units subject to review; US: 1,280 units - Foreign: 6,275 units.
Recall Details
- Product Type
- Devices
- Report Date
- May 29, 2013
- Initiation Date
- February 15, 2013
- Termination Date
- July 11, 2014
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 7,555 units subject to review; US: 1,280 units - Foreign: 6,275 units
Product Description
Molift Smart 150
Reason for Recall
The leg spreading mechanism will fail to hoist and collapse if assemble incorrectly by the user.
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.
Code Information
Art #: 0920001 batch 1-62 and 0920002 batch 1-77; Serial Number ranges 022228 to 094103 and 100015 to 12058.