ETAC A/S Recalls Molift 4-Point Sling Bars Due to Risk of Structural Failure

What Happened

ETAC A/S has initiated a voluntary recall of Molift 4-point sling bars, which serve as accessories to mobile hoists. The recall was prompted by a customer report of a mounting bolt breaking during assembly and load testing. Subsequent investigations by the firm revealed that material deformation between the lifting bar and the device arm can restrict joint mobility, preventing the equipment from functioning correctly.

Which Products Are Affected

The recall affects 25 units of the following Molift 4-point sling bar models:

• Brand Name: Molift
• Product Name: Molift 4-point sling bars (Accessory to mobile hoists)
• Model/Catalog Numbers: 1430116, 1430117, and 1430115
• Recall Number: Z-1311-2026

These products were distributed worldwide. In the United States, distribution was documented in Pennsylvania. International distribution included 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

The firm initially notified affected parties via telephone. Consumers and healthcare facilities using these specific Molift sling bar models should contact ETAC A/S regarding the defect. As the device is intended for individuals lacking the ability to stand or transfer themselves, users should ensure the equipment is inspected for proper functionality and joint mobility before further use.

Why This Matters

These sling bars are critical components of assistive hoists used to transfer individuals with limited mobility between beds, chairs, or floors. A structural failure or restricted mobility in the device joint could lead to equipment malfunction during patient handling, posing a significant safety risk to both users and caregivers.

Source

Information provided by the FDA.