Health product recall

Likorall™ Patient Lift Systems

Brand(s)
Last updated

Summary

Product
Likorall™ Patient Lift Systems
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information.

Affected products

Affected products

Lot or serial number

Model or catalogue number

Likorall™ 200

More than 10 numbers, contact manufacturer.

3121001

Likorall™ 250 S

More than 10 numbers, contact manufacturer.

3124050

Likorall™ 242 S

More than 10 numbers, contact manufacturer.

3122009

Likorall™ 242 S

More than 10 numbers, contact manufacturer.

3122010

Likorall™ 242 S

More than 10 numbers, contact manufacturer.

3122009NA

Likorall™ 242 S

More than 10 numbers, contact manufacturer.

3122010NA

Likorall™ 250 ES

More than 10 numbers, contact manufacturer.

3122502

Likorall™ 250 ES

More than 10 numbers, contact manufacturer.

3122502NA

Likorall™ 250 ES

More than 10 numbers, contact manufacturer.

3122501

Likorall™ 250 ES

More than 10 numbers, contact manufacturer.

3122501NA

Likorall™ 242 ES R2R

More than 10 numbers, contact manufacturer.

3122008NA

Likorall™ 242 ES R2R

More than 10 numbers, contact manufacturer.

3122007

Likorall™ 242 ES R2R

More than 10 numbers, contact manufacturer.

3122007NA

Likorall™ 242 ES R2R

More than 10 numbers, contact manufacturer.

3122008

Likorall™ 243 ES

More than 10 numbers, contact manufacturer.

3123001

Likorall™ 243 ES

More than 10 numbers, contact manufacturer.

3123002

Likorall™ 243 ES

More than 10 numbers, contact manufacturer.

3123001NA

Likorall™ 243 ES

More than 10 numbers, contact manufacturer.

3123002NA

Likorall™ 242 S R2R

More than 10 numbers, contact manufacturer.

3122012

Likorall™ 242 S R2R

More than 10 numbers, contact manufacturer.

3122012NA

Likorall™ 242 S R2R

More than 10 numbers, contact manufacturer.

3122011

Likorall™ 242 S R2R

More than 10 numbers, contact manufacturer.

3122011NA

Likorall™ 242 ES

More than 10 numbers, contact manufacturer.

3122006

Likorall™ 242 ES

More than 10 numbers, contact manufacturer.

3122005

Likorall™ 242 ES

More than 10 numbers, contact manufacturer.

3122006NA

Likorall™ 242 ES

More than 10 numbers, contact manufacturer.

3122005NA

Issue

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.

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - General hospital and personal use
Companies

Liko AB

Nedre Vagen 100, Lulea, Sweden, 97592

Published by
Health Canada
Audience
General public
Recall class
Type II
Recall date
Identification number
RA-82675

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