Recall Z-0105-2019— Liko AB
Class II · Terminated
Class II FDA medical device recall by Liko AB, initiated 2018-07-17, terminated 2019-04-19. FDA's recall record names no specific 510(k) clearance for this event. Product: Multirall(TM) 200Liko Strap Gripper P/N 3136250 overhead lift for patient transfer situations.. 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..
- Recalling firm
- Liko AB
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2018-07-17
- Terminated
- 2019-04-19
- Firm location
- Lulea, N/A, Sweden
Product description
Multirall(TM) 200Liko Strap Gripper P/N 3136250 overhead lift for patient transfer situations.
Reason for recall
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.