Quick Facts at a Glance
- Recall Date
- November 17, 2025
- Hazard Level
- HIGH
- Brand
- ETAC A/S
- Category
- Health & Personal Care
- Sold At
- Multiple Retailers
- Geographic Scope
- 1 states
- At-Risk Groups
- GENERAL
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- ETAC A/S
- Product type
- Patient Lifter
- Model numbers
- (1) Model/Catalog Number: M14000, UDI-DI: 05707995032270, Serial Numbers: 616606, 616604, 591003, 591002, 590906, 590901 +12 more
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
November 17, 2025
Reported by FDA DEVICE
February 11, 2026
RecallRadar source check
February 18, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
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.
What You Should Do
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact ETAC A/S or your healthcare provider for instructions. Notification method: Telephone
About This Product
The Molift Mover 205 is a patient lifting device used to assist in transferring individuals with limited mobility. It is commonly used in healthcare settings to ensure safe and comfortable transfers.
Why This Is Dangerous
The defect occurs due to material deformation between the lifting bar and arm, which can lead to bolt failure during operation. This can cause the device to malfunction, putting users at risk of injury during transfers.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
Consumers who own this device need to act quickly to ensure their safety. The risk of malfunction poses a potential danger during use, affecting patient care and safety.
Practical Guidance
How to identify if yours is affected
- Check the model number against the recalled models.
- Inspect the device for any visible issues with the lifting bar and bolts.
- Verify the serial number matches those listed in the recall.
Where to find product info
The model and serial numbers are typically located on the device's identification label, often found near the lifting mechanism.
What timeline to expect
Expect the refund processing timeline to be around 4-6 weeks after returning the product.
If the manufacturer is unresponsive
- Document all communication attempts with ETAC A/S.
- Consider contacting consumer protection agencies for further assistance.
- Keep a record of your refund request and any correspondence.
How to prevent similar issues
- When purchasing similar devices, look for safety certifications from recognized organizations.
- Check for recalls on medical devices regularly through the FDA website.
- Consult with healthcare professionals about the best lifting devices for your needs.
Documentation advice
Document all interactions with the company regarding the recall, including emails and phone calls. Keep receipts and any other purchase documentation.
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Product Details
The recall affects Molift Mover 205 models M14000, M1401, M1402, M14050, M14150, M1402-01, M14050-00, and M14001. These units were distributed worldwide, including across the United States, Australia, and several European countries. The defective devices were sold from an unspecified date.
Key Facts
- Recall Date: November 17, 2025
- Report Date: February 11, 2026
- Quantity Recalled: 95 units
- Countries Affected: Worldwide
- Manufacturer: ETAC A/S
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Safety Guide
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