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Molift Recalls 2-Point Sling Bars Due to High Injury Risk

ETAC A/S recalled 64 units of Molift 2-point sling bars on November 17, 2025. A defect in the mounting bolt can lead to failure during use. This poses serious risks for users relying on the device for mobility assistance.

Official notice
ETAC A/SHealth & Personal CareMedical Devices(1) Model/Catalog Number: 1530101UDI-DI: TBD(2) Model/Catalog Number: 1530102

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
November 17, 2025
Status
ACTIVE
Severity
8/10

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

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 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 Sling Bar
Model numbers
(1) Model/Catalog Number: 1530101, UDI-DI: TBD, (2) Model/Catalog Number: 1530102
Sold at
Multiple Retailers
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    November 17, 2025

  2. Reported by FDA DEVICE

    February 11, 2026

  3. RecallRadar source check

    February 18, 2026

  4. 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

Molift 2-point sling bars are assistive devices designed to help individuals with limited mobility transfer safely between locations like beds and wheelchairs. They are typically used in healthcare settings or home care for patients who cannot stand on their own.

Why This Is Dangerous

The hazard arises from a manufacturing defect that causes the mounting bolt to break, leading to a failure of the device during crucial transfers. This can result in falls or other serious injuries for users relying on the device for mobility assistance.

Industry Context

This recall is not part of a broader industry pattern.

Real-World Impact

The recall affects consumers who rely on these devices for safe transfers. Users must act immediately to prevent potential injuries.

Practical Guidance

How to identify if yours is affected

  1. Locate the model number on your sling bar, which should be either 1530101 or 1530102.
  2. Inspect the mounting area for any visible signs of wear or deformation.
  3. Contact your healthcare provider for assistance in determining if your device is affected.

Where to find product info

The model number is typically located on the product label or the manufacturer's documentation.

What timeline to expect

Expect a refund or replacement processing time of approximately 4-6 weeks after following the recall instructions.

If the manufacturer is unresponsive

  • Document all communication attempts with ETAC A/S.
  • Consider reaching out to consumer protection agencies for assistance.
  • Keep detailed records of your issues for reference.

How to prevent similar issues

  • Look for safety certifications such as ISO or CE when purchasing medical devices.
  • Research recalls and safety history of products before use.
  • Consult with healthcare professionals regarding safe equipment options.

Documentation advice

Keep copies of your purchase receipt, any correspondence with the manufacturer, and photographs of the product.

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Product Details

The recalled products are Molift 2-point sling bars, model numbers 1530101 and 1530102. They were distributed worldwide, including the US, and are intended as accessories to mobile hoists. No price was specified.

Reported Incidents

There is one reported incident where the bolt broke during assembly and load testing. No injuries have been disclosed, but the risk of injury remains high.

Key Facts

  • Defect in mounting bolt can break
  • High injury risk
  • Stop using immediately

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
(1) Model/Catalog Number: 1530101
UDI-DI: TBD
(2) Model/Catalog Number: 1530102
Affected States
ALL
Report Date
February 11, 2026
Recall Status
ACTIVE

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