Operating room table — Class II medical device recall Z-2585-2021
Terminated recall by Deerfield Imaging, Inc., reported 2021-10-06, distributed nationwide. ORT200/300 rotational lock may fail to function such that it cannot change states between locked and unlocked,
| Recall number | Z-2585-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Deerfield Imaging, Inc., Minnetonka, MN, United States |
| Recall initiated | 2021-08-25 |
| Classified | 2021-09-28 |
| Reported by FDA | 2021-10-06 |
| Terminated | 2024-04-30 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, JP, SE |
| Quantity | 10 units |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 00857534006356 |
| Serial numbers | 10002255, 10002841, 10002997, 10002998, 10004372, 10005456, 10005613, 10005695, 10006737, 10007377 |
| Model numbers | 114093-000 |
Product
Operating room table - Product Usage: intended for use during diagnostic examinations, radiologic procedures or surgical procedures to support and position a patient.
Reason for recall
ORT200/300 rotational lock may fail to function such that it cannot change states between locked and unlocked, due to a mechanical hardware issue.
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-2585-2021. 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.