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
- Mobile Hoist
- Model numbers
- (1) Model/Catalog Number: M1501, UDI-DI: TBD, Serial Numbers: 601005, 601002, 611506, 621101, 621106, 621104 +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 300 is a mobile hoist designed to assist individuals with mobility impairments in transferring between surfaces such as beds, chairs, and toilets. It is commonly used in healthcare settings and by caregivers at home.
Why This Is Dangerous
The hazard arises from a defect that can cause the bolt connecting the lifting bar to break, resulting in loss of functionality and potential falls. This defect compromises the safety of users who rely on the hoist for mobility.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
The recall poses a significant safety concern for individuals relying on these devices for mobility. Users must stop using the hoists immediately, which can lead to inconvenience and potential reliance on alternative assistance.
Practical Guidance
How to identify if yours is affected
- Locate the model number on your device.
- Check if it matches any of the recalled models: M1501, M1502, M1504, M15050, M15151, M15001, M15002.
- Inspect the joint area for any visible deformation.
Where to find product info
Model numbers are typically found on a label attached to the hoist's frame or on the manual.
What timeline to expect
Expect the refund process to take approximately 4-6 weeks after returning the product.
If the manufacturer is unresponsive
- Document all correspondence with the manufacturer.
- Follow up with a phone call if you do not receive a timely response.
- Consider filing a complaint with relevant consumer safety organizations.
How to prevent similar issues
- When purchasing a hoist, check for safety certifications and reviews.
- Ensure the device has a robust warranty and customer support.
- Inquire about the materials used in the product for durability.
Documentation advice
Keep copies of your purchase receipt, any emails or letters from the manufacturer, and photographs of the product as evidence.
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Product Details
The recalled models include M1501, M1502, M1504, M15050, M15151, M15001, and M15002. These devices were distributed worldwide, including the US and several European countries. They are assistive devices designed for individuals with mobility impairments.
Reported Incidents
There is one reported incident of a bolt breaking during assembly and load testing. No injuries have been reported as a result of this defect.
Key Facts
- Deformation risk between lifting bar and arm
- High hazard level identified
- Stop use immediately
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Safety Guide
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