Official recall record

Likorall™ Patient Lift Systems

What the authority reported

Baxter Corporation is issuing an urgent medical device correction for the Likorall™ ceiling-mounted overhead patient lift system due to a potential issue involving motor shaft breakage combined with reduced performance of the single fault safety (SFS) system. In rare cases where a double fault failure occurs simultaneously, with both a motor shaft breakage and reduced SFS system performance, customers have reported instances of the lift strap lowering more quickly than expected during use.

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

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