Shanghai United Imaging Healthcare Co., Ltd. recalls UIH uMI 780 PET/CT scanners due to third-party covers trapping between patient table and gantry, causing mechanical interference during scans.
Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.
UIH Technologies recalls its uMI 78:0 PET/CT scanners because third-party outer covers can get stuck between the patient table and gantry, causing mechanical interference during scans. This could lead to unsafe patient movement or equipment damage if not addressed.
Third-party outer covers can become trapped between the patient table and the scanner gantry during movement. This mechanical interference could cause the table to move unexpectedly, potentially leading to patient injury or equipment damage.
Healthcare facilities using the uMI 780 PET/CT scanners are most at risk. Patients undergoing scans with these systems may experience mechanical interference if the covers are not properly secured.
Check for the model number uMI 780 on the scanner. The serial numbers 300072, 300082, and 300098 are affected. These scanners were sold with a medical device use designation (MD, Rx Only).
Inspect if third-party outer covers are present and properly secured between the patient table and gantry.
Third-party outer covers can become trapped between the patient table and gantry, causing mechanical interference during table movement.
Check if third-party covers are present and properly secured. If not, contact UIH Technologies for guidance.
Yes, serial numbers 300072, 300082, and 300098 are affected.
We’ve drafted a message you can send UIH Technologies to request your refund or repair — edit it as you like.
Subject: Recall Z-0224-2026 — UIH Technologies UIH Technologies Hello, I own a UIH Technologies that is covered by recall Z-0224-2026 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.
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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.
