Handicare AB: Medical Device Recall in 2020 - (Recall #: Z-1943-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: June 15, 2016

Date Posted: May 20, 2020

Recall Number: Z-1943-2020

Event ID: 85362

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.

Status: Ongoing

Product Quantity: 997 units

Code Information:

All affected models

Distribution Pattern:

US and Mexico

Voluntary or Mandated:

Voluntary: Firm initiated