FDA recall Z-1943-2020

Product

EVA Floor Lifts, Model Numbers: 400, 450, 600

Reason for recall

After feedback from customers and internal suspicion, Handicare has become aware that abnormal use of Eva-lifts could lead to a deterioation in the joint of the liftarm. This could lead to injury if the joint breaks. All lifts must therefore be checked and reported back to the manuafacturer.

Distribution

US and Mexico

Key facts

Status

Ongoing

Initiation date

2016-06-15

Report date

2020-05-20

Voluntary/Mandated

Voluntary: Firm initiated

Location

Lulea, N/A, Sweden

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1943-2020