Z-0105-2019 Class II Terminated
FDA device recall Z-0105-2019 was initiated by Liko AB on July 17, 2018 and is designated Class II. 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 inj… The recall status is terminated (terminated April 19, 2019). Affected quantity: 2.
Recall Details
- Product Type
- Devices
- Report Date
- October 24, 2018
- Initiation Date
- July 17, 2018
- Termination Date
- April 19, 2019
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2
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.
Distribution Pattern
The products were distributed to the following US states: OH.
Code Information
Part Number 3136250, the manufacturing date is on the right side of the label listed as 2017-05-05.