FujiFilm recalls digital mobile X-ray systems (DR-XD1000) due to risk of serious injury from a breakable arm component. Affected units have serial numbers ending 0001-1993. Contact for repair or return.
Arm which holds the tube head in place is susceptible to breaking, if the device breaks it could potentially cause serious harm or injury to the patient and/or user.
FujiFilm is recalling its DR-XD1000 digital mobile X-ray systems because the arm holding the X-ray tube can break, potentially causing serious injury to patients or users. This recall affects units sold between 2007 and 2008 with specific serial numbers.
The arm component that holds the X-ray tube can break under stress, which might cause the X-ray tube to move unexpectedly. This could lead to serious injury to patients or users during medical imaging procedures.
Healthcare facilities using the DR-XD1000 X-ray system for medical imaging are most at risk. Patients and medical staff during exams could be injured if the arm breaks.
Check the serial number on your DR-XD1000 X-ray system. Units with last 4 digits from 0001 to 1993 were sold between 2007 and 2008.
Look for the serial number on the device; affected units end with last 4 digits between 0001 and 1993.
Reach out to FujiFilm Healthcare Americas for repair or return instructions.
The arm holding the X-ray tube can break, potentially causing serious injury to patients or users during medical imaging.
The DR-XD1000 model with serial numbers ending between 0001 and 1993.
Check the serial number; affected units have last 4 digits from 0001 to 1993.
We’ve drafted a message you can send FUJIFILM Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1470-2023 — FUJIFILM Healthcare FUJIFILM Healthcare Hello, I own a FUJIFILM Healthcare that is covered by recall Z-1470-2023 from FUJIFILM 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.
