# FDA recall Z-1308-2026

> **ETAC A/S** · Class II · device recall initiated 2025-11-17.

## Product

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;

## 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.

## Distribution

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.

## Key facts

- **Recall number:** Z-1308-2026
- **Recalling firm:** ETAC A/S
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-11-17
- **Report date:** 2026-02-11

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Gedved, N/A, Denmark

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1308-2026

## Citation

> AI Analytics. FDA recall Z-1308-2026. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1308-2026. Source: US FDA. Licensed CC0.

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