UIH Technologies recalls specific Positron Emission Tomography systems due to risk of mechanical interference from third-party covers during patient table movement. Affected models include uMI Panorama 35 MD.
Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.
UIH Technologies recalls specific Positron Emission Tomography systems where third-party outer covers can get stuck between the patient table and gantry, causing mechanical interference during movement. This could lead to safety issues during medical scans.
Third-party outer covers can get stuck between the patient table and the scanner gantry. When the table moves, this trapped cover can cause mechanical interference, potentially disrupting the scan or causing injury.
Medical facilities using the specific uMI Panorama 35 MD models are most at risk. Patients undergoing scans with these systems may be affected if covers become trapped.
Check for the model number uMI Panorama 35 MD on the device. Affected units have serial numbers 11MI410003, 11MI410004, 11MI410005, or 20MI410001.
Inspect the patient table and gantry for third-party outer covers that may be trapped between them.
The recalled model is uMI Panorama 35 MD.
Check for the model number uMI Panorama 35 MD and serial numbers 11MI410003, 11MI410004, 11MI410005, or 20MI410001.
Inspect the patient table and gantry for third-party outer covers that may be trapped between them.
We’ve drafted a message you can send UIH Technologies to request your refund or repair — edit it as you like.
Subject: Recall Z-0225-2026 — UIH Technologies UIH Technologies Hello, I own a UIH Technologies that is covered by recall Z-0225-2026 from UIH Technologies. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
