uCT 780 scanners recalled because third party covers can jam table
UIH Technologies is recalling two uCT 780 computed tomography systems because third-party outer covers can become trapped between the patient table and gantry.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: Scored 2 because the record describes mechanical interference during table movement without stating a hazard, patient consequence or reported harm.
Plain-English summary
The uCT 780 Computed Tomography X-ray System from Shanghai United Imaging Healthcare is being recalled.
Third-party outer covers can become trapped between the patient table and the gantry, causing mechanical interference during table movement.
The recall covers two units carrying UDI 06971576831050, serial numbers 684001 and 684002. The FDA has classified the action as Class II.
The enforcement record describes the interference and does not state any injury or patient consequence. Sites operating affected serial numbers should follow the firm's instructions.
The recalled product
- Product
- Shanghai United Imaging Healthcare Co., Ltd. Computed Tomography X-ray System, Model:uCT 780 MD, Rx Only
- Manufacturer
- UIH Technologies LLC
- Category
- Medical Device — CT system
- Hazard
- mechanical-interference
- third-party-accessory
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- UDI: (01)06971576831050/Serial Numbers: 684001
- 684002
Distribution
Distribution scope not specified by the agency.
Related recalls
Same category
- SevereT-Lok Bone Marrow Tray Kits Recalled for Sterility Testing Failure
FDA (Devices) · 2026-07-22
- SevereAbiomed Impella CP Introducer Kit heart pump accessory recall
FDA (Devices) · 2026-07-22
- HighOlympus Glass Body for 194 Ellik Evacuator Model 190A Sterilization Recall
FDA (Devices) · 2026-07-22
- HighOlympus Toomey Evacuator 50cc with Adaptor sterilization recall
FDA (Devices) · 2026-07-22
- SevereMedtronic Bio-Medicus Adult Cannula Kit Recalled for Foreign Material
FDA (Devices) · 2026-07-22