Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Terminated

Universal SlingBar 600 Product Number: 3156076 Used with the: Viking XS, Viking S, Viking M, Viking L Patient Lifts

FDA Recall Z-2317-2008 · Posted 2008-09-20

Recalling FirmLiko AB
Recall StatusTerminated
Product CodeFSA
Date Initiated2008-07-01
Date Terminated2015-07-17

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.

Firm 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.

Root Cause

Component design/selection

Distribution Pattern

Nationwide

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

↑