Getinge recalls Volista light systems due to potential for light systems to fall in operating rooms. Affected models include Volista, Volista Access, Volista Access II, and Volista Standop OR Light System with specific model numbers.
A potential for a light system to fall in the operating room.
Getinge is recalling several models of Volista light systems because there's a risk of the light system falling in the operating room. This could cause injury to medical staff or patients if the light falls and hits someone.
The light system could fall from its mounting in the operating room, potentially causing injury to people nearby. This risk is higher in environments where the light is used frequently and where there's limited space to avoid the fall.
Healthcare professionals and patients using the Volista light systems in operating rooms are most at risk. The recall affects specific models sold in the U.S. by Getinge.
Check for the product names: Volista, Volista Access, Volista Access II, or Volista Standop OR Light System. Look for the specific model numbers listed in the recall notice, which include catalog numbers like ARDROL309001A and others.
Identify your light system model by checking the product name and catalog numbers listed in the recall notice.
Reach out to Getinge directly for assistance with the recall or to confirm if your model is affected.
The recall is due to a potential risk that the light system could fall in the operating room, which could cause injury to medical staff or patients.
The affected models include Volista, Volista Access, Volista Access II, and Volista Standop OR Light System with specific model numbers listed in the recall notice.
No, the recall does not require immediate stoppage. Healthcare professionals should use caution and check if their model is affected before taking any action.
We’ve drafted a message you can send Getinge to request your refund or repair — edit it as you like.
Subject: Recall Z-0758-2024 — Getinge Getinge Hello, I own a Getinge that is covered by recall Z-0758-2024 from Getinge. 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.
