Arjo recalls Enterprise 5000X, 8000X, 9000X and Citadel medical beds with IndiGo Drive modules due to unintended wheel movement. Affected units have specific serial numbers and UDI/DI codes.
Unintended movement of bed wheels
Arjo is recalling certain medical beds that may move unexpectedly when wheels are turned. This could cause falls or injuries for patients or staff using the beds.
The bed wheels can move unexpectedly when the bed is adjusted, potentially causing the bed to shift or tip. This could lead to falls or injuries for people using the bed.
Healthcare facilities and medical staff who use the recalled Arjo beds are most at risk. Patients using these beds could also be affected if they fall.
Check for the model names: Enterprise 5000X, Enterprise 8000X, Enterprise 9000X, or Citadel. Look for the UDI/DI code 0505609734548 or specific serial numbers listed in the recall notice.
Identify if your bed is one of the affected models: Enterprise 5000X, Enterprise 8000X, Enterprise 9000X, or Citadel.
Check the serial number on the bed's label; affected units have specific serial numbers listed in the recall notice.
The bed wheels can move unexpectedly when the bed is adjusted, potentially causing the bed to shift or tip and leading to falls or injuries.
Check if your bed is one of the affected models (Enterprise 5000X, Enterprise 8000X, Enterprise 9000X, or Citadel) and has a serial number from the list provided in the recall notice.
Check the bed model and serial number to confirm if it's affected. If it is, contact Arjo directly for further instructions.
We’ve drafted a message you can send Arjo to request your refund or repair — edit it as you like.
Subject: Recall Z-0611-2024 — Arjo Arjo Hello, I own a Arjo that is covered by recall Z-0611-2024 from Arjo. 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.