FDA Device recall Z-1263-2018
IMRIS ORT100 Table, Part Numbers: (a) 110470-000 (b) 110470-600
- FDA Device
- Class II
- terminated
- Published 2018-04-04
On 2018-04-04 the FDA classified a Class II recall of IMRIS ORT100 Table, Part Numbers: (a) 110470-000 (b) 110470-600 by Deerfield Imaging, citing the Operating Room Table may drift while in use, which could potentially result in unintended movement of the table.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1263-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-02-23 |
| Published | 2018-04-04 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Deerfield Imaging |
| Distribution | n/a |
Product
IMRIS ORT100 Table, Part Numbers: (a) 110470-000 (b) 110470-600
Reason
The Operating Room Table may drift while in use, which could potentially result in unintended movement of the table.
Identifiers
| code_info | (a) 110470-000, Serial Numbers: 10002845, 10002341, 10003629, 10003801, 10002654, 10002795, 10002796, 10002847, 100038…(a) 110470-000, Serial Numbers: 10002845, 10002341, 10003629, 10003801, 10002654, 10002795, 10002796, 10002847, 10003830, 10003243, 10003241, 10002607, 10002848, 10005651, 10007348, 10007424, 10004250, 10004439, 10004576, 10006438, 100030007, 10006887, 10006886 (b) 110470-600, Serial Numbers: 10003244, 10003064, 10003065 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1263-2018%22
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