FDA Medical Device Recalls (openFDA)
Liko, Inc.: UNO 100 EM/EE Patient Lift
- Recall number
- Z-0876-05
- Recalling firm
- Liko, Inc.
- Product
- UNO 100 EM/EE Patient Lift
- Status
- Terminated
- Initiated
- 2004-09-24
- Posted
- 2005-06-08
- Terminated
- 2007-06-20
- Reason
- Incorrect length support screws may cause patient lift failure
- Root cause
- Other
- Action
- Liko notified Peridot Group by letter dated 9/29/04 of the recall. All Canadian distributors, including Peridot, will contact and inspect and replace bolts at user sites.
- Quantity
- 398 units
- Distribution
- Canada
- Lot, serial or model codes
- Serial Number: Range 7090602-7093161
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FNG
- Firm FEI
- 3001451524
- Firm city
- Franklin
- Firm state
- MA
- Firm country
- not on file
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