Class II — Raye's Inc.
| Recalling firm | RAYE'S, Inc dba Sizewise Manufacturing a wholly owned subsid |
|---|---|
| Registered facility | View this company's 5 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | 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. |
| Product | SW Bari Lift & Transfer, Model Number 38060000 |
| Quantity | 1,149 units |
| Distribution | Worldwide distribution - US Nationwide and the countries of Australia, UK. |
| Initiated | 2024-01-25 |
| Classified | 2024-04-18 |
| Recall number | Z-1595-2024 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Raye's Inc. (Z-1595-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/93887/
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