Class II — Med-Mizer, Inc.
| Recalling firm | MED-MIZER, INC |
|---|---|
| Registered facility | MED-MIZER, INC (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Risk of boom pivot failing due to the nut securing the boom becoming loose and the bolt to be unsecure to the flange on the side. |
| Product | Sit to Stand STS500 Patient Lift |
| Quantity | 37 units |
| Distribution | Awaiting consignee list from the recalling firm. |
| Initiated | 2023-02-03 |
| Classified | 2023-03-02 |
| Recall number | Z-1205-2023 |
| 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 — Med-Mizer, Inc. (Z-1205-2023).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/91695/
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