Human Care HC Sweden AB is recalling 10 Altair and Roomer S patient lifts because the hanger bar, which supports the patient, may come loose during use. This recall affects Altair 330 lbs and Roomer S 220 kg models manufactured between May 2023 and October 2023. These devices were distributed across several states including Texas, Illinois, Oklahoma, and California.
If the hanger bar detaches while a patient is being lifted or moved, the patient could fall from the device, potentially leading to serious physical injuries.
Manufacturer instructions for device safety.
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.
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.