ETAC A/S: Medical Device Recall in 2026 - (Recall #: Z-1310-2026)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2026.

Data Source: FDA.

Product Description:

Brand Name: Molift Product Name: Molift 2-point sling bars (Accessory to mobile hoists) Model/Catalog Numbers: (1) 1530101, (2) 1530102 Product Description: The mobile hoist is an assistive device intended for alleviation of, or compensation for, a functional, impairment due to an injury or disability. The device is designed for an individual lacking the ability to stand up and transfer themselves to / from a bed, the floor, a wheelchair, a chair, a toilet or similar due to reduced mobility or physical strength.

Product Classification:

Class II

Date Initiated: November 17, 2025

Date Posted: February 11, 2026

Recall Number: Z-1310-2026

Event ID: 98087

Reason for Recall:

A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this customer complaint, it became clear that the defect occurs as a result of deformation of the materials involved between the lifting bar and the arm of the device. Such deformation can lead to limited mobility in the joint, which prevents proper functionality of the equipment.

Status: Ongoing

Product Quantity: 64 units

Code Information:

(1) Model/Catalog Number: 1530101; UDI-DI: TBD; (2) Model/Catalog Number: 1530102; UDI-DI: TBD;

Distribution Pattern:

Worldwide - US Nationwide distribution in the state of PA and the countries of Australia, Czech Republic, Finland, France, Germany, Israel, Italy, Japan, New Zealand, Norway, Poland, Qatar Spain, Sweden, Switzerland, UK.

Voluntary or Mandated:

Voluntary: Firm initiated