Z-2316-2008

Universal SlingBar 450 Product Number: 3156075 Used with the: Viking XS, Viking S, Viking M, Viking L Patient...

Name: Z-2316-2008 Universal SlingBar 450 Product Number: 3156075 Used with the: Viking XS, Viking S, Viking M, Viking L Patient...
Creator: Liko AB
Published: 2008-07-01
License: https://open.fda.gov/license/

Liko AB / initiated 2008-07-01 / Terminated / root cause: design

FDA source

Liko AB began a recall of Universal SlingBar 450 Product Number: 3156075 Used with the: Viking XS, Viking S, Viking M, Viking L Patient Lifts on 2008-07-01. The reason FDA records is "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". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as design.

Recall record

Recall number: Z-2316-2008
Status: Terminated
Initiated: 2008-07-01
Posted: 2008-09-20
Terminated: 2015-07-17
Recalling firm: Liko AB
Product: Universal SlingBar 450 Product Number: 3156075 Used with the: Viking XS, Viking S, Viking M, Viking L Patient Lifts
Product code: FSA Lift, Patient, Non-Ac-Powered
Reason for recall: 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.
Root cause tag: design
FDA root cause: Component design/selection
Action: 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.
Distribution: Nationwide
Product codes and lots: Affected serial numbers on sling bars: 1200101-1245680, 121204-121499, and 12222407-12225241

Product code FSA

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-10-07, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)