Raye's Inc. SW Bari Lift & Transfer, Model Number 38060000 Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
SW Bari Lift & Transfer, Model Number 38060000
Brand
Raye's Inc.
Lot Codes / Batch Numbers
UDI/DI 00845699001040, All serial numbers
Products Sold
UDI/DI 00845699001040, All serial numbers
Raye's Inc. is recalling SW Bari Lift & Transfer, Model Number 38060000 due to Retrospective engineering analysis against current ISO standards for hoists has determined: 1. The device cannot physically perform at maximum documen. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
Sizewise Manufacturing issued an URGENT Voluntary Medical Device Recall to its consignees on 01/29/2024 by letter. The notice explained the issue, potential risk, and requested the discontinuation of use and disposal of the device. The firm sent a follow-up notice on 03/07/2024 asking the distributors to further notify their customers (users of the device).
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026