GE Healthcare recalls AMX Navigate Mobile X-Ray Systems with unexpected column motion during parking. Affected models include AMXNV2000001WK, AMXNV2000:002WK, DF2401600003WK. Stop using immediately to prevent potential injury.
An unexpected column motion while attempting to park the column on the AMX Navigate mobile X-ray system.
GE Healthcare is recalling certain AMX Navigate Mobile X-Ray Systems due to unexpected column motion when attempting to park the column. This hazard could lead to injury if the system moves unexpectedly during use.
The system's column may move unexpectedly when trying to park it, which could cause the system to tip over or shift. This movement might injure patients or staff during medical procedures.
Healthcare facilities using the recalled AMX Navigate Mobile X-Ray Systems are most at risk. Patients and staff could be injured if the column moves unexpectedly during operation.
Check for the model numbers AMXNV2000001WK, AMXNV2000002WK, or DF2401600003WK on the system. The recall applies to specific mobile X-ray systems sold by GE Healthcare.
Discontinue use of the affected AMX Navigate Mobile X-Ray Systems to prevent unexpected column motion.
The affected models are AMXNV2000001WK, AMXNV2000002WK, and DF2401600003WK.
The recall is due to an unexpected column motion when attempting to park the column on the AMX Navigate mobile X-ray system, which could cause injury.
Stop using the affected models immediately to prevent potential injury from unexpected column motion.
We’ve drafted a message you can send GE Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-2590-2021 — GE Healthcare GE Healthcare Hello, I own a GE Healthcare that is covered by recall Z-2590-2021 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.