IMRIS ORT300 — Class II medical device recall Z-1266-2018
Terminated recall by Deerfield Imaging, Inc., reported 2018-04-04. The Operating Room Table may drift while in use, which could potentially result in unintended movement of the
| Recall number | Z-1266-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Deerfield Imaging, Inc., Minnetonka, MN, United States |
| Recall initiated | 2018-02-23 |
| Classified | 2018-03-28 |
| Reported by FDA | 2018-04-04 |
| Terminated | 2019-09-12 |
| Countries outside the US | AU, CA, CN, DE, SE |
| Quantity | 13 units |
| Serial numbers | 10002255, 10002841, 10002996, 10002997, 10002998, 10004372, 10004515, 10005456, 10005612, 10005613, 10005695, 10007377, 10007411 |
| Model numbers | 114093-000, 114093-600 |
Product
IMRIS ORT300, Removable Operating Room Table, Part Numbers: (a) 114093-000 (b) 114093-600
Reason for recall
The Operating Room Table may drift while in use, which could potentially result in unintended movement of the table.
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-1266-2018. 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.