Z-0277-06

UNO 102 Patient Lift

Name: Z-0277-06 UNO 102 Patient Lift
Creator: Liko, Inc.
Published: 2005-11-14
License: https://open.fda.gov/license/

Liko, Inc. / initiated 2005-11-14 / Terminated

FDA source

Liko, Inc. began a recall of UNO 102 Patient Lift on 2005-11-14. The reason FDA records is "Incorrect length leg pin bolts may cause patient lift failures". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0277-06
Status: Terminated
Initiated: 2005-11-14
Posted: 2005-12-13
Terminated: 2008-02-20
Recalling firm: Liko, Inc.
Product: UNO 102 Patient Lift
Product code: FSA Lift, Patient, Non-Ac-Powered
Reason for recall: Incorrect length leg pin bolts may cause patient lift failures
FDA root cause: Other
Action: Liko Inc. initiated the recall to Distributors of the Recall on 11/14/05 via UPS. Direct customers will be notified by letter on /about 12/1/05.
Quantity in commerce: 663 units
Distribution: Nationwide
Product codes and lots: Serial Numbers: 33590-42291

Product code FSA

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)