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 | Terminated |
| Reason | Under certain conditions, when pivoting bed to the extreme left there are situations where the wire/cables may become pinched. A failure would result in the resident requiring to be transferred to a different bed until repairs can be made |
| Product | PR1000 Pivot Rehab Bed AC powered adjustable bed. |
| Quantity | 230 units |
| Distribution | The products were distributed to the following US states: AR, AZ, FL, GA, IA, ID, IL, IN, KY, ME, MI, MN, MO, NC, ND, NE, NM, NY, OH, OK, PA, SC, SD, TN, TX, VA, WA, and WI. The products were distributed to the following foreign countries: Canada, China, and Denmark. |
| Initiated | 2018-07-25 |
| Classified | 2018-09-17 |
| Terminated | 2019-10-11 |
| Recall number | Z-3183-2018 |
| 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-3183-2018).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/80832/
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