GE OEC recalls OEC 9900 Systems with 9-inch Image Intensifier that may detach during movement, causing injury. Affected units have specific serial numbers. Stop using immediately to prevent fractures or bruising.
Image intensifiers on systems, used to provide fluoroscopic/digital spot images can become detached if the systems encounter a large impact force when moved, which may result in the image intensifier falling, which could lead to injuries such as fractures, hematoma, contusion, bruise, pain.
GE OEC is recalling OEC 9900 Systems with 9-inch Image Intensifiers that can become detached if the system is moved after a large impact. This detachment could lead to injuries like fractures, bruising, or pain. Affected units have specific serial numbers listed in the recall.
The image intensifier can become detached if the system experiences a large impact force during movement. This detachment may cause the image intensifier to fall, potentially leading to injuries such as fractures, bruising, or pain.
Medical professionals using OEC 9900 Systems with 9-inch Image Intensifiers are most at risk. The recall applies to specific units with the listed serial numbers.
Check the serial numbers listed in the recall: ES-2700, ESXXXL00081, and other specific serial numbers provided in the record. The product is used in medical imaging systems.
Discontinue use of the OEC 9900 System with the affected 9-inch Image Intensifier to prevent detachment and injury.
OEC 9900 Systems with 9-inch Image Intensifiers.
The affected units have specific serial numbers listed in the recall, including ES-2700, ESXXXL00081, and many others as detailed in the record.
The image intensifier can become detached if the system is moved after a large impact, potentially causing it to fall and result in injuries like fractures, bruising, or pain.
We’ve drafted a message you can send GE OEC to request your refund or repair — edit it as you like.
Subject: Recall Z-2277-2023 — GE OEC GE OEC Hello, I own a GE OEC that is covered by recall Z-2277-2023 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.
