Liko AB Alvik Universal SlingBar 600 Product Number: 3156076 Used with the: Viking XS, Viking S, Viking M, Viking L Patient Lifts Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Universal SlingBar 600 Product Number: 3156076 Used with the: Viking XS, Viking S, Viking M, Viking L Patient Lifts
Brand
Liko AB Alvik
Lot Codes / Batch Numbers
Affected serial numbers on sling bars: 1200101-1245680, 121204-121499, and 12222407-12225241
Products Sold
Affected serial numbers on sling bars: 1200101-1245680, 121204-121499, and 12222407-12225241
Liko AB Alvik is recalling Universal SlingBar 600 Product Number: 3156076 Used with the: Viking XS, Viking S, V due to A component securing the Universal SlingBar to the patient lift, may experience a nut unthreading resulting in the sling bar detaching from the lift c. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
A component securing the Universal SlingBar to the patient lift, may experience a nut unthreading resulting in the sling bar detaching from the lift causing the patient to fall.
Recommended Action
Per FDA guidance
Liko North America ,the US Distributor, notified accounts by letter dated June 30, 2008 and provided a Field Safety Notice with Safety Inspection Procedures to performed on the lift prior to use. Replacement slingbars are being provided. If you have questions, contact the Liko product distributor in your country. Contact information can be found at www.liko.com/int/distributors.asp.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026