Z-1117-2007

Liko Universal Sling Bar 450 Quick Release Hook (QRH) Product Number: 3156085

Name: Z-1117-2007 Liko Universal Sling Bar 450 Quick Release Hook (QRH) Product Number: 3156085
Creator: Liko, Inc.
Published: 2007-06-13
License: https://open.fda.gov/license/

Liko, Inc. / initiated 2007-06-13 / Terminated / root cause: design

FDA source

Liko, Inc. began a recall of Liko Universal Sling Bar 450 Quick Release Hook (QRH) Product Number: 3156085 on 2007-06-13. The reason FDA records is "Sling bar may have a center bolt break at the adapter while in use". As of 2026-09-10, the recall status on record is Terminated, and MDM tags the root cause as design.

Recall record

Recall number: Z-1117-2007
Status: Terminated
Initiated: 2007-06-13
Posted: 2007-07-23
Terminated: 2015-10-20
Recalling firm: Liko, Inc.
Product: Liko Universal Sling Bar 450 Quick Release Hook (QRH) Product Number: 3156085
Product code: FRW Scale, Patient
Reason for recall: Sling bar may have a center bolt break at the adapter while in use
Root cause tag: design
FDA root cause: Component design/selection
Action: Liko Inc notified distributors and end users by letter on 6/13/07.
Quantity in commerce: 22
Distribution: Nationwide
Product codes and lots: Serial Numbers: 1200101 through 1201281

Product code FRW

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)