Med-Riser MR600 Patient Lift — Class II medical device recall Z-1204-2023
Ongoing recall by Med-Mizer, Inc., reported 2023-03-08. Risk of boom pivot failing due to the nut securing the boom becoming loose and the bolt to be unsecure to the
| Recall number | Z-1204-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Med-Mizer, Inc., Batesville, IN, United States |
| Recall initiated | 2023-02-03 |
| Classified | 2023-03-02 |
| Reported by FDA | 2023-03-08 |
| Quantity | 241 units |
| UPC / GTIN / UDI-DI | 00852195007308 |
| Serial numbers | MR600000, MR600001, MR600002, MR600003, MR600004, MR600005, MR600006, MR600007, MR600008, MR600009, MR600010, MR600011, MR600012, MR600013, MR600014, MR600015, MR600016, MR600017, MR600018, MR600019, MR600020, MR600021, MR600022, MR600023, MR600024 and 216 more |
Product
Med-Riser MR600 Patient Lift
Reason for recall
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.
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-1204-2023. 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.