GE OEC recalls OEC 9900 Elite mobile fluoroscopy systems due to manufacturing issues causing potential oil leaks and loss of imaging capability. Affected units have specific serial numbers listed in the recall notice.
Due to manufacturing issue of insufficient sealing of X-ray tubes and can result in a potential oil leak and loss of fluoroscopic imaging capability.
GE OEC is recalling its OEC 9900 Elite mobile fluoroscopy systems because of a manufacturing defect that may cause oil leaks and loss of imaging capability. This could affect medical procedures requiring precise X-ray imaging.
The system has a manufacturing issue with insufficient sealing of X-ray tubes, which can lead to oil leaks. This may cause the fluoroscopic imaging capability to fail during medical procedures, potentially affecting diagnostic accuracy.
Healthcare facilities using the OEC 9900 Elite mobile fluoroscopy system for medical procedures are most at risk. Patients undergoing imaging procedures with this equipment may be affected if the system malfunctions.
Check for the OEC 9900 Elite mobile fluoroscopy system with serial numbers listed in the recall notice, including E2-0345, E2-7031, E2-1862, ES-0942, E9-1101, E9-2173, E9-2706, E2-5146, E2-1777, E2XXXX05533, and other specific codes mentioned in the recall.
Review the serial numbers listed in the recall notice to determine if your unit is affected.
The recall is due to a manufacturing issue with insufficient sealing of X-ray tubes, which can cause oil leaks and loss of fluoroscopic imaging capability.
Check the serial numbers listed in the recall notice to see if your unit is affected. If it is, contact GE OEC for further instructions.
The recall states potential oil leaks and loss of imaging capability, but does not mention risks of serious injury or death. The hazard level is low risk.
We’ve drafted a message you can send GE OEC to request your refund or repair — edit it as you like.
Subject: Recall Z-0705-2025 — GE OEC GE OEC Hello, I own a GE OEC that is covered by recall Z-0705-2025 from GE OEC. 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.
