PR1000 Pivot Rehab Bed AC powered adjustable bed — Class II medical device recall Z-3183-2018
Terminated recall by Med-Mizer, Inc., reported 2018-09-26, distributed in AR, AZ, FL, GA, IA, ID, IL, IN…. Under certain conditions, when pivoting bed to the extreme left there are situations where the wire/cables may
| Recall number | Z-3183-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Med-Mizer, Inc., Batesville, IN, United States |
| Recall initiated | 2018-07-25 |
| Classified | 2018-09-17 |
| Reported by FDA | 2018-09-26 |
| Terminated | 2019-10-11 |
| Distributed | 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, WI |
| Countries outside the US | CA, CN, DK |
| Quantity | 230 units |
Product
PR1000 Pivot Rehab Bed AC powered adjustable bed.
Reason for recall
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
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-3183-2018. 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.