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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Home Healthcare

Molift Mover Hoists and Sling Bars Recalled for Lifting Bar Joint Defect

Agency Publication Date: February 5, 2026
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Summary

ETAC A/S is recalling approximately 255 Molift brand mobile hoists and sling bar accessories, including the Molift Mover 205 and 300 models. The recall was initiated after a mounting bolt broke during assembly and load testing due to material deformation between the lifting bar and the device arm. This defect can cause limited mobility in the joint and prevent the equipment from functioning correctly, which is critical for an assistive device designed to transfer individuals with physical impairments.

Risk

The mounting bolt for the lifting bar can break or the joint can seize due to material deformation, potentially causing the lifting mechanism to fail while in use. This poses a risk of injury to patients being transferred and their caregivers if the hoist cannot be safely operated or if the lifting bar detaches.

What You Should Do

  1. Identify if you have a Molift Mover 205, Molift Mover 300, or Molift 2-point/4-point sling bar accessory.
  2. Check your device for the following model numbers: M14000, M1401, M1402, M14050, M14150, M1402-01, M14050-00, M14001, M1501, M1502, M1504, M15050, M15151, M15001, M15002, 1530101, 1530102, 1430116, 1430117, or 1430115.
  3. Check the serial number on your device label against the list of affected units. See the Affected Products section below for the full list of affected codes.
  4. Stop using the recalled device immediately to prevent potential injury.
  5. Contact the manufacturer, ETAC A/S, or your local distributor to arrange for a return, replacement, or correction of the equipment.
  6. Call the FDA consumer hotline at 1-888-463-6332 if you have additional questions regarding this medical device recall.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: Molift Mover 205by Molift
Model / REF:
M14000
M1401
M1402
M14050
M14150
M1402-01
M14050-00
M14001
Serial Numbers (95):
616606
616604
591003
591002
590906
590901
590904
590903
590902
591001
604101
604005
591703
591007
591006
591005
591004
615105
615104
615103
615102
615101
604004
604003
604002
604001
614202
614201
591702
591701
616603
615106
590905
593302
593301
593303
612507
612506
612508
612505
612503
620702
612504
612502
612501
593304
593305
620703
620701
612601
UDI:
05707995032270

95 units distributed.

Product: Molift Mover 300by Molift
Model / REF:
M1501
M1502
M1504
M15050
M15151
M15001
M15002
Serial Numbers (71):
601005
601002
611506
621101
621106
621104
621105
621102
611505
611504
611503
611502
611501
601008
611507
601007
601006
601001
621103
601003
601004
611409
611408
611407
611406
611405
611404
611403
611402
611401
611412
611411
611410
600902
600901
611303
611302
611301
586003
586001
585905
585903
585902
585901
598605
586101
585904
603602
591401
586002
UDI:
TBD

71 units distributed.

Product: Molift 2-point sling barsby Molift
Model / REF:
1530101
1530102
UDI:
TBD

64 units distributed.

Product: Molift 4-point sling barsby Molift
Model / REF:
1430116
1430117
1430115
UDI:
TBD

25 units distributed.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98087
Status: Active
Manufacturer: ETAC A/S
Sold By: Authorized Medical Equipment Distributors
Manufactured In: Denmark
Units Affected: 4 products (95 units; 71; 64 units; 25 units)
Distributed To: Pennsylvania

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.