FDAClass IJune 1, 2022

Sara Plus Active Floor Lift recall

Sara Plus Active Floor Lift

Why was Sara Plus Active Floor Lift recalled?

The device may emit smoke or ignite.

What should I do if I have this product?

Review the official FDA enforcement record for current 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?

Model Numbers: HEP0001, HEP0001-AU, HEP0001-BR, HEP0001-CN, HEP0001-JP, HEP0001-UK, HEP0001-US, HEP1001, HEP1001-AU, HEP1001CON4869, HEP1001-US, HEP2001, HEP2001-BR, HEP2001-CN, HEP2001-UK

Product
Sara Plus Active Floor Lift
Recalling firm
ARJOHUNTLEIGH POLSKA Sp. z.o.o.
Quantity
4449 devices
Distribution
US Nationwide and Worldwide distribution
Recall date
June 1, 2022
Classification
Class I
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls