# FDA recall Z-1486-2024

> **Human Care Hc Sweden Ab** · Class II · device recall initiated 2024-02-23.

## Product

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

## Reason for recall

Patient lift hanger bar may come loose, which could potentially pose risks to patients.

## Distribution

US Nationwide distribution in the states of TX, IL, OK, CA.

## Key facts

- **Recall number:** Z-1486-2024
- **Recalling firm:** Human Care Hc Sweden Ab
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-02-23
- **Report date:** 2024-04-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Stockholm, N/A, Sweden

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1486-2024

## Citation

> AI Analytics. FDA recall Z-1486-2024. Retrieved 2026-08-12 from https://api.ai-analytics.org/recall/Z-1486-2024. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
