CLASS II ONGOING Device recall · Reported 17 Apr 2024 · FDA Enforcement Report
Altair w/o Hanger Bar recalled by Human Care Hc Sweden Ab
Human Care Hc Sweden Ab is recalling Altair w/o Hanger Bar, distributed nationwide in the US. The recall was initiated on 23 Feb 2024 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1486-2024
- FDA event ID
- 94140
- Recalling firm
- Human Care Hc Sweden Ab, Stockholm, N/A
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 23 Feb 2024
- FDA classified
- 5 Apr 2024
- Reported
- 17 Apr 2024
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Other Reasons
- Device type
- Wheelchairs, Beds & Lifts
Timeline
| 23 Feb 2024 | Recall initiated by company | |
| 5 Apr 2024 | Classified by FDA | +42 days |
| 17 Apr 2024 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Patient lift hanger bar may come loose, which could potentially pose risks to patients.
Product as listed by the FDA
Altair 330 lbs w/o Hanger Bar, REF: 55200H-NA, 55220H-NA, and Roomer S 220 kg w/o Hanger Bar, REF: 55300H-NA, patient lifts
Where it was distributed
US Nationwide distribution in the states of TX, IL, OK, CA.
Questions about this recall
Why was it recalled?
Patient lift hanger bar may come loose, which could potentially pose risks to patients.
Which lots are affected?
UDI-DI: 7331599999943 Products manufactured between May 2023 and October 2023. Serial Numbers: 236229060002, 236229060005, 236232010015, 236229070004, 236232010006, 236229060003, 236229060009, 236229060006, 236232010005, 236232010003
Where was it sold?
US Nationwide distribution in the states of TX, IL, OK, CA.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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