SW Bari Lift & Transfer — Class II medical device recall Z-1595-2024
Ongoing recall by Raye's Inc., reported 2024-04-24, distributed nationwide. Retrospective engineering analysis against current ISO standards for hoists has determined: 1. The device cann
| Recall number | Z-1595-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Raye's Inc., Hays, KS, United States |
| Recall initiated | 2024-01-25 |
| Classified | 2024-04-18 |
| Reported by FDA | 2024-04-24 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, GB |
| Quantity | 1,149 units |
| UPC / GTIN / UDI-DI | 00845699001040 |
| Model numbers | 38060000 |
Product
SW Bari Lift & Transfer, Model Number 38060000
Reason for recall
Retrospective engineering analysis against current ISO standards for hoists has determined: 1. The device cannot physically perform at maximum documented weight specifications when a factor of safety of two times the maximum load is applied. 2. The device is not equipped with a safety device to ensure a person with disability would not fall in the event of a single-fault condition of the lifting device.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1595-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.