Brand Name: Molift Product Name: Molift Mover 205 Model/Catalog Number: (1) M14000, (2) M1401, (3)
Pending LLM rewrite. Source: FDA_DEVICE Z-1308-2026.
Severity not yet assessed
We have not scored this recall against our rubric yet, so we are not showing a severity rating or our usual guidance. The agency’s own notice below is the authoritative source — read it first.
Plain-English summary
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.
The recalled product
- Product
- Brand Name: Molift Product Name: Molift Mover 205 Model/Catalog Number: (1) M14000, (2) M1401, (3) M1402, (4) M14050, (5) M14150, (6) M1402-01, (7) M14050-00 (8) M14001;
- Manufacturer
- ETAC A/S
- Category
- Medical Device — Devices
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (20)
- (1) Model/Catalog Number: M14000
- UDI-DI: 05707995032270
- Serial Numbers: 616606
- 616604
- 591003
- 591002
- 590906
- 590901
- 590904
- 590903
- 590902
- 591001
- 604101
- 604005
- 591703
- 591007
- 591006
- 591005
- 591004
- 615105
Distribution
Distributed nationwide across the United States.
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