U.S. Food and Drug Administration - CDRH Mobile
Skip NavigationFDA Logo links to FDA home pageCenter for Devices and Radiological Health, U.S. Food and Drug AdministrationHHS Logo links to Department of Health and Human Services website
FDA Home Page | CDRH Home Page | Search | A-Z Index U.S. Food and Drug AdministrationCenter for Devices and Radiological Health Questions?
horizonal rule

FDA > CDRH > Medical Device Recalls > Class I Recall - Faaborg Patient Lifts

Medical Device Recalls
Class I Recall - Faaborg Patient Lifts

Date Recall
Initiated:
 January 21, 2004
Product:
 Faaborg battery operated patient lift,
Person Lift PL, VL and Solution/Nordic Series.
Use:
 Patient lifts are mechanical sling-like devices used to lift and transport patients from one place to another, as from a bed to a wheelchair or bath. They are used in hospitals and nursing homes in the care of the elderly and handicapped persons.
Recalling Firm:
 Moving Solutions, Inc.
2550 Wisconsin Ave.
Downers Grove, IL 60515
Reason for Recall:
 Excessive wear of the hanger bar bolt, which secures the hanger bar to the lift arm of the patient lift, will cause the bolt to break. When the bolt breaks, the hanger bar is no longer secured to the lift arm, which will cause the patient to fall. The hanger bar may also fall on the patient, which could result in serious injury, even death.
Public Contact:
 Andrew M. Ringo
Director, Moving Solutions, Inc.
(630) 963-9693
FDA District:
 Chicago
FDA Comment:
 Facilities should stop using these lifts until the problem is corrected. Use of these uncorrected lifts exposes patients to a reasonable probability that the product will cause serious injury or death.
 


For additional information on this product recall, see

U.S. Department of Justice News Release at:
http://www.fda.gov/bbs/topics/news/2004/doj0628.html

FDA News at:
http://www.fda.gov/bbs/topics/NEWS/2004/NEW01032.html

FDA Enforcement Report located at: http://www.fda.gov/bbs/topics/enforce/2004/ENF00840.html. Scroll down to "Recalls and Field Corrections: Devices – Class I".

Updated November 15, 2004

horizonal rule

CDRH Home Page | CDRH A-Z Index | Contact CDRH | Accessibility | Disclaimer
FDA Home Page | Search FDA Site | FDA A-Z Index | Contact FDA | HHS Home Page

Center for Devices and Radiological Health / CDRH