ORT300, operating room table recall
IMRIS Imaging Inc recalled ORT300, operating room table on September 2, 2026 because of the linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between locked and unlocked state. It was sold nationwide.
Why it was recalled
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.
What's recalled
ORT300, operating room table, ORT300 Modular Table Main Unit Assy Part Numbers 114093-000 and 114093-600
Quantity: 13 units
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- IMRIS Imaging Inc, Chaska, MN
- Date
- Severity
- Class II
the product could cause temporary or reversible health problems. - Where sold
- Nationwide
Worldwide distribution - US Nationwide and the countries of Canada, China, Japan, Sweden. - Status
- Ongoing
- Recall number
- Z-3034-2026
- Source
- U.S. Food and Drug Administration
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