OFFICIAL-SOURCE RECALL · CANADA
Likorall™ Patient Lift Systems Recall: Baxter Corporation is issuing an urgent medical
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Is your product affected?
- Brand
- See official notice
- Product
- Likorall™ Patient Lift Systems
- Manufacturer
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The barcode may identify the product type, while the recall may apply only to certain lots, dates or variants. Check all identifiers listed in the official recall.
Why this product was recalled
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.
Hazard
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.
Official recall notice
Likorall™ Patient Lift Systems
Agency: Health Canada
Official publication date: September 24, 2026
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