Z-0875-05

UNO 102 EM/EE/ES Patient Lift

Name: Z-0875-05 UNO 102 EM/EE/ES Patient Lift
Creator: Liko, Inc.
Published: 2004-09-24
License: https://open.fda.gov/license/

Liko, Inc. / initiated 2004-09-24 / Terminated

FDA source

Liko, Inc. began a recall of UNO 102 EM/EE/ES Patient Lift on 2004-09-24. The reason FDA records is "Incorrect length support screws may cause patient lift failure". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0875-05
Status: Terminated
Initiated: 2004-09-24
Posted: 2005-06-08
Terminated: 2007-06-20
Recalling firm: Liko, Inc.
Product: UNO 102 EM/EE/ES Patient Lift
Product code: FNG Lift, Patient, Ac-Powered
Reason for recall: Incorrect length support screws may cause patient lift failure
FDA 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 in commerce: 21 units
Distribution: Canada
Product codes and lots: Serial Numbers: Range 33590-42291

Product code FNG

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 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)