GE Healthcare recalls Precision 600FP radiographic systems due to potential monitor suspension detachment causing patient or operator injury.
GE Healthcare has become aware of a potential safety issue associated with the improper installation of the Precision 600FP monitor suspension. A partial detachment of the monitor suspension could result in potential injury to a patient or operator.
GE Healthcare is recalling certain Precision 600FP radiographic systems because improper installation might cause the monitor suspension to partially detach, potentially injuring patients or operators. This is a safety issue that requires attention to prevent harm.
The monitor suspension may partially detach if not installed correctly, which could lead to injury during medical procedures. This risk occurs when the system is used for radiographic or fluoroscopic imaging on patients or operators.
Healthcare facilities using the recalled Precision 600FP systems for medical imaging are most at risk. Qualified doctors and technologists who operate these systems could be affected.
Check for the specific serial numbers listed in the recall notice. These systems were sold for medical imaging use by qualified healthcare professionals.
Identify if your system has one of the listed serial numbers from the recall notice.
Improper installation of the monitor suspension could cause partial detachment, potentially injuring patients or operators during medical imaging procedures.
Check if your system has one of the specific serial numbers listed in the recall notice.
The recall notice does not specify a remedy, so contact GE Healthcare directly for guidance.
We’ve drafted a message you can send GE Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1101-2021 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-1101-2021 from GE Healthcare. 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.
