Lulea, N/A, Sweden
Liko AB recalls
1 recall recorded since 2018, most recently on 17 July 2018. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Terminated Class II Medical devices
- Recall started
- 17 July 2018
- Terminated
- 19 April 2019
- 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.
- Distribution
- The products were distributed to the following US states: OH.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0105-2019
- Multirall(TM) 200Liko Strap Gripper P/N 3136250 overhead lift for patient transfer situations.
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.