Liko Multirall 200Liko Strap Gripper Overhead Lift Recall
Liko AB is recalling two Multirall 200Liko Strap Gripper overhead lifts due to potential assembly errors that could cause patient falls.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a risk-of-harm product (potential patient falls and injury) where no specific injuries have been reported yet, fitting the criteria for a High severity score.
Plain-English summary
Liko AB is recalling two units of the Multirall 200Liko Strap Gripper (P/N 3136250) overhead lift. These devices are used for patient transfer situations. The specific units subject to recall were manufactured on May 5, 2017, and were distributed to Ohio.
The recall was initiated because the products may have been assembled incorrectly. If an incorrectly assembled product is used for patient transport, it could allow the patient to fall, resulting in potential injury.
Consumers and healthcare facilities should stop using the affected units immediately. The manufacturing date is listed on the right side of the label as 2017-05-05. Users should contact Liko AB for further instructions on how to proceed with the recall.
The recalled product
- Product
- Multirall(TM) 200Liko Strap Gripper P/N 3136250 overhead lift for patient transfer situations.
- Manufacturer
- Liko AB
- Category
- Medical Device — Patient Lifts
- Affected units
- 2
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- Part Number 3136250
- the manufacturing date is on the right side of the label listed as 2017-05-05.
Distribution
Distributed in 1 state:
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