FDA Device recall Z-0976-2018
IMRIS T2X Table, Part Number 109682-600
- FDA Device
- Class II
- terminated
- Published 2018-03-21
On 2018-03-21 the FDA classified a Class II recall of IMRIS T2X Table, Part Number 109682-600 by Deerfield Imaging, citing the rotational locking mechanisms on the ORT 100/ T2X tables can become disengaged or unlocked 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-0976-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-02-20 |
| Published | 2018-03-21 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Deerfield Imaging |
| Distribution | n/a |
Product
IMRIS T2X Table, Part Number 109682-600
Reason
The rotational locking mechanisms on the ORT 100/ T2X tables can become disengaged or unlocked while in use which could potentially result in unintended movement of the table.
Identifiers
| code_info | Serial Numbers: 10000239, 10001306, 10000983, 10000982, 10000233, 10001119, 10001192, 10002375, 10003623, 10003623, 05…Serial Numbers: 10000239, 10001306, 10000983, 10000982, 10000233, 10001119, 10001192, 10002375, 10003623, 10003623, 05 002, 10003634, 10001118, 10001188, 10001340, 10003638 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
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Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0976-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.