FDAAugust 11, 2021device
Stretch Leveller Model Number: 3156200 - The combination of this products allows the user to easily adjust/control the center of gravity during lift of patient.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Stretch Leveller has the potential to lose the function of maintaining a patient in the horizontal position when lifting and in motion. When this function is lost the patient can slide backwards and potentially may fall out of the Oct lift sheet back onto the surface it is being lifted from.
What to do
FDA enforcement status: Ongoing
Brands named
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Recall history
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