IMRIS ORT300 Removable Operating Room Table — Class II medical device recall Z-1218-2018
Terminated recall by Deerfield Imaging, Inc., reported 2018-04-04. The rotational locking mechanisms on the ORT 200/300 tables fail to operate such that it cannot change states
| Recall number | Z-1218-2018 |
|---|---|
| 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 | 2018-03-27 |
| Reported by FDA | 2018-04-04 |
| Terminated | 2019-08-27 |
| Countries outside the US | CA, CN, DE, FR, JP, QA, SE |
| Quantity | 13 units |
| Serial numbers | 10002255, 10002841, 10002996, 10002997, 10002998, 10004372, 10004515, 10005456, 10005612, 10005613, 10005695, 10007377, 10007411 |
Product
IMRIS ORT300 Removable Operating Room Table, 50-60 Hz Version is intended for use during diagnostic examinations or surgical procedures to support and position a patient.
Reason for recall
The rotational locking mechanisms on the ORT 200/300 tables fail to operate such that it cannot change states between locked and unlocked.
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-1218-2018. 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.