FDA Medical Device Recalls (openFDA)
Liko, Inc.: Liko Universal Slingbar 450 (aluminum) used with the Viking L Patient Lift
- Recall number
- Z-0791-06
- Recalling firm
- Liko, Inc.
- Product
- Liko Universal Slingbar 450 (aluminum) used with the Viking L Patient Lift
- Status
- Terminated
- Initiated
- 2006-01-09
- Posted
- 2006-04-26
- Terminated
- 2006-10-25
- Reason
- 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.
- 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
- 38 units
- Distribution
- IL, MA, MO, PA, TN,
- Lot, serial or model codes
- Serial Numbers: 7200202 - 7200216; 7200244 - 7200245; 7200250 - 7200257; 7200260 - 7200262 Expanded recall: Viking L: Serial Nimbers: 7200201 through 7200284
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FSA
- Firm FEI
- 3001451524
- Firm city
- Franklin
- Firm state
- MA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28