FDA Medical Device Recalls (openFDA)
Liko AB: Multirall(TM) 200Liko Strap Gripper P/N 3136250 overhead lift for patient transfer situations.
- Recall number
- Z-0105-2019
- Recalling firm
- Liko AB
- Product
- Multirall(TM) 200Liko Strap Gripper P/N 3136250 overhead lift for patient transfer situations.
- Status
- Terminated
- Initiated
- 2018-07-17
- Posted
- not on file
- Terminated
- 2019-04-19
- Reason
- The products manufactured on 5/5/17 may be assembled incorrectly. If the incorrectly assembled products is used for patient transport, this could allow the patient to fall, resulting in potential injury to the patient.
- Root cause
- Storage
- Action
- The customer was contacted via telephone on 7/17/18 to notify them of the recall. An Urgent Field Safety Notice notification letter was sent to the customer on 7/19/18.
- Quantity
- 2
- Distribution
- The products were distributed to the following US states: OH.
- Lot, serial or model codes
- Part Number 3136250, the manufacturing date is on the right side of the label listed as 2017-05-05.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- FSA
- Firm FEI
- 6884
- Firm city
- Lulea
- Firm state
- not on file
- Firm country
- Sweden
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