UIH Technologies recalls uCT 760 MD CT scanners due to third-party covers trapping between patient table and gantry, potentially causing mechanical interference during scans. Affected units have specific serial numbers.
Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.
UIH Technologies is recalling uCT 760 MD CT scanners because third-party outer covers can get stuck between the patient table and the machine's gantry during scans. This could cause mechanical interference that might affect the scan or patient safety.
Third-party outer covers can become trapped between the patient table and the gantry during table movement. This mechanical interference might cause the table to move incorrectly or stop, potentially affecting scan quality or patient safety.
Healthcare facilities using the uCT 760 MD CT scanners with serial numbers 600229 through 604008 are most at risk. Patients undergoing scans with these machines may experience mechanical interference.
Check for the model uCT 760 MD with serial numbers 600229 to 604008. These scanners were sold as Rx-only devices by UIH Technologies.
Identify your scanner's serial number from the list: 600229, 600232, 600271, 600282, 604001, 604002, 604003, 604004, 604005, 604006, 604008
The recall is due to third-party outer covers potentially getting trapped between the patient table and gantry during scans, causing mechanical interference.
Check your scanner's serial number against the list: 600229 to 604008. If it matches, contact UIH Technologies for guidance.
The recall record does not specify a fix or remedy; affected users should contact UIH Technologies directly.
We’ve drafted a message you can send UIH Technologies to request your refund or repair — edit it as you like.
Subject: Recall Z-0219-2026 — UIH Technologies UIH Technologies Hello, I own a UIH Technologies that is covered by recall Z-0219-2026 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.
