Arjo recalls Enterprise 5000X, 8000X, 9000X and Citadel medical beds assembled with IndiGo Drive modules due to unintended wheel movement. Affected units have specific serial numbers listed in the recall notice.
Unintended movement of bed wheels
Arjo is recalling certain medical beds (Enterprise 5000X, 8000X, 9000X, and Citadel models) that were assembled with IndiGo Drive Assistance modules. The beds may experience unintended movement of the wheels, which could cause instability during use.
The wheels on these beds may move unexpectedly when the bed is in use, potentially causing the bed to shift or tip. This could lead to falls or injuries for patients or staff if the bed is not properly secured.
Healthcare facilities and medical professionals who own or use the affected Arjo medical beds. Patients using these beds could be at risk if the wheels move unexpectedly.
Check if your Arjo medical bed has the following model names: Enterprise 5000X, Enterprise 8000X, Enterprise 9000X, or Citadel. Affected units were assembled with IndiGo Drive Assistance modules and have 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 if your bed's serial number matches any of the listed serial numbers in the recall notice.
The beds may experience unintended movement of the wheels when in use, which could cause instability and potential injury.
Check if your bed is one of the affected models (Enterprise 5000X, 8000X, 9000X, or Citadel) and verify the serial number against the list provided in the recall notice.
No action is needed if your bed is not listed in the recall notice.
We’ve drafted a message you can send Arjo to request your refund or repair — edit it as you like.
Subject: Recall Z-0612-2024 — Arjo Arjo Hello, I own a Arjo that is covered by recall Z-0612-2024 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.
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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.
