ETAC A/S recalls Molift 2-point sling bars (models 1530101, 1530102) due to material deformation causing joint failure. Affected users should contact for remedy.
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.
ETAC A/S recalls Molift 2-point sling bars (models 1530101 and 1530102) because material deformation during use can cause joint failure, preventing proper function. This affects people who rely on the device for mobility assistance.
The device's lifting bar can deform between the bar and the arm during use, causing limited mobility in the joint. This deformation prevents the equipment from functioning properly, which could lead to difficulties in moving safely.
People who use Molift 2-point sling bars for mobility assistance, such as those with limited ability to stand or transfer between surfaces. Those most at risk are individuals who depend on the device for daily mobility tasks.
Check for Molift 2-point sling bars with model numbers 1530101 or 1530102. These accessories are sold with mobile hoists for mobility assistance.
Reach out to ETAC A/S for instructions on how to proceed with the recall.
The recall is due to material deformation causing joint failure, which prevents proper functionality of the device.
Model numbers 1530101 and 1530102.
If you use Molift 2-point sling bars for mobility assistance, the deformation could cause joint failure, making the device less effective.
We’ve drafted a message you can send Molift to request your refund or repair — edit it as you like.
Subject: Recall Z-1310-2026 — Molift Molift Hello, I own a Molift that is covered by recall Z-1310-2026 from Molift. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
