ETAC A/S Recalls Molift 2-Point Sling Bars Due to Structural Bolt Failure Risk
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ETAC A/S has issued a voluntary recall for 64 Molift 2-point sling bars after reports of mounting bolts breaking, which could lead to equipment failure during patient transfers.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on April 6, 2026 and geographically references Worldwide. Its severity classification of "high" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, MedicalDevices.
What Happened
ETAC A/S has initiated a voluntary recall of Molift 2-point sling bars, which serve as accessories to mobile hoists. The recall follows a customer report involving a mounting bolt that broke during assembly and load testing. A subsequent investigation by the firm determined that the defect is caused by material deformation between the lifting bar and the arm of the device. This deformation can restrict joint mobility, preventing the equipment from functioning properly.
Which Products Are Affected
The recall affects 64 units of the following products:
- Brand Name: Molift
- Product Name: Molift 2-point sling bars (Accessory to mobile hoists)
- Model/Catalog Numbers: 1530101 and 1530102
- Recall Number: Z-1310-2026
These units were distributed worldwide, including nationwide in the United States (specifically in Pennsylvania), and in Australia, Czech Republic, Finland, France, Germany, Israel, Italy, Japan, New Zealand, Norway, Poland, Qatar, Spain, Sweden, Switzerland, and the United Kingdom.
What You Should Do
ETAC A/S initiated the recall process via telephone notifications to affected parties. Consumers and healthcare providers who have these specific model numbers should contact ETAC A/S for guidance on the return or repair process. The firm is located at Parallelvej 3, Gedved, Denmark.
Why This Matters
Mobile hoists are critical assistive devices for individuals with physical impairments or reduced mobility. A structural failure, such as a broken mounting bolt on a sling bar, can cause the device to fail during use, potentially leading to patient injury during transfers.
Source
Information provided by the FDA.
Original source: FDA Official Notice ↗
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