Atlas FDA

Molift Air 205, Molift Air 205 Propulsion, Molift Air IRC, Molift Air 205 IRC Propulsion, Molift Air 300, Molift Air 300

FDA device recall Z-2291-2016 · posted 2016-07-26 · Terminated

Recall details

Recalling firm
Moller Vital
Reason for recall
Potential for the bolt on the suspension coupling on the Molift Air to come loose from the housing.
Action taken
Moller Vital sent a Field Safety Corrective Action on June 22, 2016. Field correction instructions were provided to affected consignees. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to read the instruction, and return the recipient confirmation, report all serial numbers distributed in their region/country to Etac Supply Gjovik, order the upgrade kit from Etac Supply Gjovik, Customers were also instructed to follow up with the customers and users and confirm that all hoists in their market are upgraded. Customers with questions were instructed to contact Etac Supply Gjovik.at molift.qa@etac.com.
Root cause
Device Design
Status
Terminated
Product code
FSA
Quantity affected
516 units (374 US)
Distribution
Worldwide Distribution - US (nationwide) and Internationally to SZ, TR, BE, CH, DE, DK, ES, FI, FR, GB, IS LV, NL, NO, SE, SI, AU, CN, IL, JP, NZ, IN, QA, PE, AE
Date initiated
2016-06-24
Date posted
2016-07-26
Date terminated
2017-06-23
Location
Gjovik, Norway

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