ETAC A/S: Device Recall

Recall #Z-1308-2026 · 11/17/2025

Class II: Risk

Recall Details

Recall Number
Z-1308-2026
Classification
Class II
Product Type
Device
Recalling Firm
ETAC A/S
Status
Ongoing
Date Initiated
11/17/2025
Location
Gedved, N/A, Denmark
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
95 units

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.

Product Description

Brand Name: Molift Product Name: Molift Mover 205 Model/Catalog Number: (1) M14000, (2) M1401, (3) M1402, (4) M14050, (5) M14150, (6) M1402-01, (7) M14050-00 (8) M14001;

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.

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.