Recall Z-1343-2013— Moller Vital
Class II · Terminated
Class II FDA medical device recall by Moller Vital, initiated 2013-02-15, terminated 2014-07-11. FDA's recall record names no specific 510(k) clearance for this event. Product: Molift Smart 150. Reason: The leg spreading mechanism will fail to hoist and collapse if assemble incorrectly by the user..
- Recalling firm
- Moller Vital
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2013-02-15
- Terminated
- 2014-07-11
- Firm location
- Gjovik, N/A, Norway
Product description
Molift Smart 150
Reason for recall
The leg spreading mechanism will fail to hoist and collapse if assemble incorrectly by the user.
Data sourced from openFDA. This site is unofficial and independent of the FDA.