Z-0790-06

Liko Universal Slingbar 450 (aluminum) used with the Viking M Patient Lift

Name: Z-0790-06 Liko Universal Slingbar 450 (aluminum) used with the Viking M Patient Lift
Creator: Liko, Inc.
Published: 2006-01-09
License: https://open.fda.gov/license/

Liko, Inc. / initiated 2006-01-09 / Terminated

FDA source

Liko, Inc. began a recall of Liko Universal Slingbar 450 (aluminum) used with the Viking M Patient Lift on 2006-01-09. The reason FDA records is "The swivel adapter which is mounted directly above the slingbar's split center bolt could be removed and allow the slingbar to be improperly mounted directly into the aluminum link arm. This could cause an unsafe...". As of 2026-09-10, the recall status on record is Terminated.

Recall record

Recall number: Z-0790-06
Status: Terminated
Initiated: 2006-01-09
Posted: 2006-04-26
Terminated: 2006-10-25
Recalling firm: Liko, Inc.
Product: Liko Universal Slingbar 450 (aluminum) used with the Viking M Patient Lift
Product code: FSA Lift, Patient, Non-Ac-Powered
Reason for recall: The swivel adapter which is mounted directly above the slingbar's split center bolt could be removed and allow the slingbar to be improperly mounted directly into the aluminum link arm. This could cause an unsafe transfer. Patient may fall.
FDA root cause: Other
Action: Liko notified Distributors of the recall by letter on 1/9/06 via UPS and provided replacement Slingbars Version 2. Expanded Recall: On 6/20/06, Liko sent a 2nd recall letter expanding the recall to additonal serial numbers via Certified Mail.
Quantity in commerce: 67 units
Distribution: IL, MA, MO, PA, TN,
Product codes and lots: Serial Numbers: 7100102 - 7100104; 7100109 7100147 - 7100159 7100179 - 7100182 7100257 - 7100261 EXPANDED RECALL: Viking M: Serial Numbers: 7100101 through Z-7100381

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)