Getinge recalls Maquet Blueline Series 30/80 OR Light Systems with specific model numbers due to potential for light systems to fall in operating rooms. Affected units include BLUE 30 and BLUE 80 models with catalog numbers starting with ARD569015111A.
A potential for a light system to fall in the operating room.
Getinge is recalling Maquet Blueline Series 30/80 OR Light Systems that could fall in the operating room. This hazard poses a risk of injury to healthcare workers during surgery.
The light system could fall in the operating room due to instability in its mounting. This poses a risk of injury to healthcare workers if the light falls during surgery, potentially causing lacerations or other injuries.
Healthcare facilities using the recalled Maquet Blueline Series 30/80 OR Light Systems are most at risk, particularly surgical teams where the light system could fall during procedures.
Check for model numbers starting with 'BLUE 30' or 'BLUE 80' with catalog numbers like ARD569015111A, ARD569014111A, or ARD569064112C. These systems were sold with specific model numbers listed in the recall notice.
Identify the model number on your light system, which should match the catalog numbers listed in the recall notice (e.g., ARD569015111A).
Reach out to Getinge for guidance on next steps if your light system is affected by the recall.
The light system could fall in the operating room, posing a risk of injury to healthcare workers during surgery.
Affected models include BLUE 30 and BLUE 80 with catalog numbers starting with ARD569015111A, ARD569014111A, and others listed in the recall notice.
The recall does not require immediate stop use; however, healthcare facilities should check if their light system is affected and contact Getinge for guidance.
We’ve drafted a message you can send Getinge to request your refund or repair — edit it as you like.
Subject: Recall Z-0770-2024 — Getinge Getinge Hello, I own a Getinge that is covered by recall Z-0770-2024 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.
