FDA recall, , Moderate risk
Molift Mover 205, Mover 300 and Sling Bars
The Molift Mover 205, Mover 300, and sling bars can have a broken bolt that limits joint mobility.
Summary by Recall Canary from the FDA notice
What happened
ETAC A/S, of Gedved, Denmark, recalled Molift 2-point sling bars, Molift Mover 205, Molift 4-point sling bars, and Molift Mover 300 after a customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. The defect occurs as a result of deformation of the materials involved between the lifting bar and the arm of the device, which can lead to limited mobility in the joint, which prevents proper functionality of the equipment.
The company began the recall on November 17, 2025, and the FDA added it to its Enforcement Report on February 5, 2026. The products were distributed in the state of Pennsylvania and in Australia, Czech Republic, Finland, France, Germany, Israel, Italy, Japan, New Zealand, Norway, Poland, Qatar, Spain, Sweden, Switzerland, and the UK.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
4 products
Affected if its UDI-DI or model/catalog number is listed.
A UDI-DI is the device identifier printed with the barcode on the device label.
Molift Mover 205
- UDI-DI
- 05707995032270
- Model/Catalog number
- (1) M14000(2) M1401(3) M1402(4) M14050(5) M14150(6) M1402-01(7) M14050-00 (8) M14001
Molift 2-point sling bars (Accessory to mobile hoists)
- Model/Catalog number
- (1) 1530101(2) 1530102
Molift 4-point sling bars (Accessory to mobile hoists)
- Model/Catalog number
- 1430116
- 1430117
- 1430115
Molift Mover 300
- Model/Catalog number
- (1) M1501(2) M1502(3) M1504(4) M15050(5) M15151(6) M15001(7) M15002
Recall details
- Company began the recall
- Sold in
Worldwide - US Nationwide distribution in the state of Pennsylvania and the countries of Australia, Czech Republic, Finland, France, Germany, Israel, Italy, Japan, New Zealand, Norway, Poland, Qatar Spain, Sweden, Switzerland, UK.
- Company
- ETAC A/SGedved, Denmark
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98087
- Recall numbers
- Z-1308-2026 to Z-1311-2026
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Listed on Recall Canary
