DeviceSignal · Recall classified

IMRIS Imaging Inc

FDA classified a device recall on 2026-08-26 · Class II · Z-3033-2026

EventRecall classified
Effective2026-08-26
ClassificationClass II

On 2026-08-26 the FDA classified a device recall from IMRIS Imaging Inc as Class II. Product: ORT200, operating room table, including the ORT200 Covered Table Assembly, Reconditioned…. Recall Z-3033-2026. The firm initiated it on 2026-08-06. This reports the classification FDA published on that date.

Reported facts

Recall number
Z-3033-2026
Classification
Class II
Classified on
2026-08-26
Initiated on
2026-08-06
Firm
IMRIS Imaging Inc
Reason
The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between locked and unlocked state. This may pose a risk of injury to the patient if unintended rotational movement occurs during a procedure.
Product
ORT200, operating room table, including the ORT200 Covered Table Assembly, Reconditioned, Part Number 113821-600 and the ORT200 50/60Hz Covered Table Assy V2 Part Number 114148-000

Every field above is as fda_device_enforcement published it. Nothing on this page is our interpretation.

Provenance

Source
fda_device_enforcement
Source record
Z-3033-2026
Snapshot hash
ab5ada73bf212eb52a548aab0968a0fcee42807c61b0350e60e24bb6e2beed72
Source URL
https://download.open.fda.gov/device/enforcement/device-enforcement-0001-of-0001.json.zip
Observed
2026-09-08T16:22:09.483Z
Transform
fda_device_enforcement_to_recall v1
Event rule
fda_device_recall_classified v1
Event key
3c6d524018d8d14951323f98469da95101c099fcc0be10f630d49f411499d2f8
Signal type
device_recall.classified

Source terms that apply

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Data provided by the U.S. Food and Drug Administration (https://open.fda.gov)