Recall Z-1351-2019— Moller Vital
Class II · Ongoing
Class II FDA medical device recall by Moller Vital, initiated 2019-02-04. FDA's recall record names no specific 510(k) clearance for this event. Product: Molift 2-Point sling bar, an accessory for Molift Mover 205. Item nos. 1430016 1430017 1430021. Reason: The firm has received 7 reports of malfunction for the device in which the hooks have broken off, potentially leading the sling to slip out of the sling bar and causing the patient to fall..
- Recalling firm
- Moller Vital
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2019-02-04
- Firm location
- Gjovik, Norway
Product description
Molift 2-Point sling bar, an accessory for Molift Mover 205. Item nos. 1430016 1430017 1430021
Reason for recall
The firm has received 7 reports of malfunction for the device in which the hooks have broken off, potentially leading the sling to slip out of the sling bar and causing the patient to fall.
Data sourced from openFDA. This site is unofficial and independent of the FDA.