The Recall Desk
HighFDA (Devices)·Z-1308-2026·Announced 2026-02-11

[pending] Brand Name: Molift Product Name: Molift Mover 205 Model/Catalog Number: (1) M14000, (2) M1401, (3)

Pending LLM rewrite. Source: FDA_DEVICE Z-1308-2026.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: Pending LLM scoring against the rubric.

Plain-English summary

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.

The recalled product

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;
Manufacturer
ETAC A/S

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (20)

  • (1) Model/Catalog Number: M14000
  • UDI-DI: 05707995032270
  • Serial Numbers: 616606
  • 616604
  • 591003
  • 591002
  • 590906
  • 590901
  • 590904
  • 590903
  • 590902
  • 591001
  • 604101
  • 604005
  • 591703
  • 591007
  • 591006
  • 591005
  • 591004
  • 615105

Distribution

Distributed nationwide across the United States.