Class II U.S. Food and Drug Administration

Etac A/S Brand Name: Molift Product Name: Molift Mover 205 Model/ recall: A customer experienced that during assembly and load testing of the device

Recall published 9 months ago

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 hazard: Lead or heavy metal content

Lead is the reason for this notice. The important thing is removing the source and asking about a blood test, in that order.

What the notice says: 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.

Why it matters: The product exceeds the federal limit on lead or another heavy metal. Lead harms the developing brain, and the damage builds quietly from small repeated exposures rather than arriving as a single dramatic poisoning.

Symptoms and when to call a doctor

The CDC states there is no known safe level of lead in a child’s blood, and that most children with elevated levels show no symptoms at all. That is why a blood lead test, not a symptom check, is the way to find out. Ask your paediatrician about testing if a child has handled, mouthed or worn the product regularly. Where symptoms do appear they are non-specific — irritability, poor appetite, stomach pain, tiredness, constipation or a drop in attention and learning.

This page is general information, not medical advice. If you feel unwell, a clinician who can see you is the only person able to judge your case.

Recall details

Recall number
Z-1308-2026
Published
February 11, 2026
Risk level
Class II
Status
Ongoing
Issued by
U.S. Food and Drug Administration
Brand
Etac A/S
Product type
Medical devices
Units affected
95 units
Distribution
Nationwide
Made in
Denmark
Lot / code info
(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, 615104, 615103, 615102, 615101, 604004, 604003, 604002, 604001, 614202, 614201, 591702, 591701, 616603, 615106, 590905; (2) Model/Catalog Number: M1401; UDI-DI: 05707995032270; Serial Numbers: 593302, 593301, 593303, 612507, 612506, 612508, 612505, 612503, 620702, 612504, 612502, 612501, 593304, 593305, 620703, 620701; (3) Model/Catalog Number: M1402; UDI-DI: 05707995032270; Serial Numbers: 612601; (4) Model/Catalog Number: M14050; UDI-DI: 05707995032270; Serial Numbers: 590801, 596701, 585701, 584501, 591801, 604405, 604406, 604402, 604404, 604403, 604401, 604303, 604302, 604301; (5) Model/Catalog Number: M14150; UDI-DI: 05707995032270; Serial Numbers: 585811, 585810, 585809, 585808, 585806, 585805, 585804, 585803, 585801, 596604, 596603, 596602, 596601, 596611, 596610, 596609, 596608, 596607, 596606, 596605, 585807, 585802; (6) Model/Catalog Number: M1402-01; UDI-DI: 05707995032270; Serial Numbers: 612701, 612703, 612702; (7) Model/Catalog Number: M14050-00; UDI-DI: 05707995032270; Serial Numbers: 584307; (8) Model/Catalog Number: M14001; UDI-DI: 05707995032270; Serial Numbers: 603501, 599801, 599802, 604202, 604201;
UPC codes
05707995032270

Products covered by this recall

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;

Check your product

The notice names 29 codes you can read straight off the package. Type the one printed on yours and the list below narrows to it.

UPC / barcode

Read the twelve digits under the barcode on the package.

  • 05707995032270

Model or item number

On the rating label, the box or the instruction sheet.

  • M14000
  • M1401
  • M1402
  • M14050
  • M14150
  • M1402-01
  • M14050-00
  • M14001

Serial number

On the rating plate, often next to the date of manufacture.

  • 616606
  • 616604
  • 591003
  • 591002
  • 590906
  • 593302
  • 593301
  • 593303
  • 612507
  • 612506
  • 612601
  • 590801
  • 596701
  • 585701
  • 584501
  • 591801
  • 585811
  • 585810
  • 585809
  • 585808

Codes are lifted verbatim from the FDA — Device enforcement notice. A code that is missing here may still be covered — the official notice is the complete list.

What to do about Lead

Etac A/S — Lead is the reason for this notice. The important thing is removing the source and asking about a blood test, in that order.

  1. Take the product away from children and stop using it — do not keep it for decoration where a child can reach it.
  2. Wash the hands of anyone who has been handling it, and wipe down the surfaces it has been sitting on.
  3. Ask your paediatrician whether a blood lead test is warranted, especially for a child under six or anyone pregnant.
  4. Do not sand, scrape, burn or break the item up; that turns a contained hazard into dust you can breathe.

How the remedy works

CPSC recalls specify one of three remedies, and which one you get is not negotiable — but how smoothly it goes often is.

  • A refund means the purchase price back, sometimes prorated by age for durable goods. Ask how they calculated it if the figure looks low.
  • Return shipping is the company’s cost. If you are asked to pay it, push back.
  • A repair kit is shipped free and is designed to be fitted at home; if you cannot fit it, ask whether they will arrange installation.
  • A replacement is usually the current model, not the recalled one. Confirm the replacement is not itself under recall.

Company contact: ETAC A/S — Parallelvej 3, Gedved

The official notice

This page summarises a notice published by U.S. Food and Drug Administration. The agency notice is the authoritative version — read it before you act, and treat it as the final word if anything here looks different.

Open the FDA — Device enforcement record U.S. Food and Drug Administration recalls

Questions people ask about this recall

Why was Etac A/S medical devices recalled?

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. 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…

How do I know if I have the recalled product?

Match the codes printed on your package against the notice: UPC 05707995032270; model number M14000, M1401, M1402. If the code on your package is not on that list, your unit is outside the recall.

What should I do with it right now?

Take the product away from children and stop using it — do not keep it for decoration where a child can reach it.

Can I get my money back?

A refund means the purchase price back, sometimes prorated by age for durable goods. Ask how they calculated it if the figure looks low.

Where was the recalled product sold?

It was distributed nationwide.

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