Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

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.

ยฉ 2026 Go Backs. All rights reserved.

Medium RiskFDA Device
Medical Devices/Home Healthcare

Human Care Hc Sweden Ab: Patient Lift Hanger Bars Recalled for Risk of Coming Loose

Agency Publication Date: April 5, 2024
Share:
Sign in to monitor this recall

Summary

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.

Risk

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.

What You Should Do

  1. Check your patient lift to see if it is an Altair 330 lbs (REF: 55200H-NA or 55220H-NA) or a Roomer S 220 kg (REF: 55300H-NA).
  2. Locate the serial number on the device's identification label and verify if it matches one of the following affected numbers: 236229060002, 236229060005, 236232010015, 236229070004, 236232010006, 236229060003, 236229060009, 236229060006, 236232010005, or 236232010003.
  3. Check the manufacturing date to see if the unit was produced between May 2023 and October 2023.
  4. Immediately contact your healthcare provider or Human Care HC Sweden AB for further instructions regarding the safety and inspection of the hanger bar mechanism.
  5. For additional information, contact the FDA's medical device recall line at 1-888-463-6332 or visit www.fda.gov/medical-devices/medical-device-recalls.

Your Remedy Options

๐Ÿ“‹Other Action

Manufacturer instructions for device safety.

How to: Contact your healthcare provider or the manufacturer for further instructions and potential refund

Affected Products

Product: Altair 330 lbs w/o Hanger Bar
Model / REF:
55200H-NA
55220H-NA
UPC Codes:
7331599999943
Lot Numbers:
236229060002
236229060005
236232010015
236229070004
236232010006
236229060003
236229060009
236229060006
236232010005
236232010003
Date Ranges: May 2023 - October 2023
Product: Roomer S 220 kg w/o Hanger Bar
Model / REF:
55300H-NA
UPC Codes:
7331599999943
Lot Numbers:
236229060002
236229060005
236232010015
236229070004
236232010006
236229060003
236229060009
236229060006
236232010005
236232010003
Date Ranges: May 2023 - October 2023

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 94140
Status: Active
Manufacturer: Human Care Hc Sweden Ab
Sold By: Specialty medical equipment distributors
Manufactured In: Sweden
Units Affected: 10
Distributed To: Texas, Illinois, Oklahoma, California

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.