Z-1486-2024 Class II Ongoing
FDA device recall Z-1486-2024 was initiated by Human Care Hc Sweden Ab on February 23, 2024 and is designated Class II. Reason for recall: Patient lift hanger bar may come loose, which could potentially pose risks to patients. The recall status is ongoing. Affected quantity: 10.
Recall Details
- Product Type
- Devices
- Report Date
- April 17, 2024
- Initiation Date
- February 23, 2024
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 10
Product Description
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 Pattern
US Nationwide distribution in the states of TX, IL, OK, CA.
Code Information
UDI-DI: 7331599999943 Products manufactured between May 2023 and October 2023. Serial Numbers: 236229060002, 236229060005, 236232010015, 236229070004, 236232010006, 236229060003, 236229060009, 236229060006, 236232010005, 236232010003