Liko, Inc. Liko Universal Slingbar 450 (aluminum) used with the Viking M Patient Lift Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Liko Universal Slingbar 450 (aluminum) used with the Viking M Patient Lift
Brand
Liko, Inc.
Lot Codes / Batch Numbers
Serial Numbers: 7100102 - 7100104
Products Sold
Serial Numbers: 7100102 - 7100104; 7100109 7100147 - 7100159 7100179 - 7100182 7100257 - 7100261 EXPANDED RECALL: Viking M: Serial Numbers: 7100101 through Z-7100381
Liko, Inc. is recalling Liko Universal Slingbar 450 (aluminum) used with the Viking M Patient Lift due to 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 d. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
IL, MA, MO, PA, TN
Page updated: Jan 10, 2026