Class II
Medical Device Recall: ORT300, operating room table, ORT300 Modular Table Main Unit Assy Part Numbers 114093-000 and 114093-600
IMRIS Imaging Inc · August 6, 2026
Reason for Recall
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.
Distribution
Worldwide distribution - US Nationwide and the countries of Canada, China, Japan, Sweden.
States Affected
NATIONWIDE
Quantity Affected
13 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-3034-2026
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.