FDAClass IIMay 20, 2020

EVA Floor Lifts recall

EVA Floor Lifts, Model Numbers: 400, 450, 600

Why was EVA Floor Lifts recalled?

After feedback from customers and internal suspicion, Handicare has become aware that abnormal use of Eva-lifts could lead to a deterioation in the joint of the liftarm. This could lead to injury if the joint breaks. All lifts must therefore be checked and reported back to the manuafacturer.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

All affected models

Product
EVA Floor Lifts, Model Numbers: 400, 450, 600
Recalling firm
Handicare AB
Quantity
997 units
Distribution
US and Mexico
Recall date
May 20, 2020
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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