FDA Medical Device Recalls (openFDA)
Liko AB: Universal SlingBar 450 with Quick-release Hook Product Number: 3156085 Used in combination with all lifts from Liko, i.e. mobile lifts and overhead lifts
- Recall number
- Z-2319-2008
- Recalling firm
- Liko AB
- Product
- Universal SlingBar 450 with Quick-release Hook Product Number: 3156085 Used in combination with all lifts from Liko, i.e. mobile lifts and overhead lifts
- Status
- Terminated
- Initiated
- 2008-07-01
- Posted
- 2008-09-20
- Terminated
- 2015-07-17
- Reason
- 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
- 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.
- Quantity
- not on file
- Distribution
- Nationwide
- Lot, serial or model codes
- Affected serial numbers on sling bars: 1200101-1245680, 121204-121499, and 12222407-12225241
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FSA
- Firm FEI
- 6884
- Firm city
- Lulea
- Firm state
- not on file
- Firm country
- Sweden
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28