Getinge recalls specific Maquet Orchide OR Light Systems models due to potential falling risk in operating rooms. Affected units include OHDII FHD QL VP01 and other variants with unique identifiers. Consumers should check their model numbers and contact Getinge for details.
A potential for a light system to fall in the operating room.
Getinge is recalling specific Maquet Orchide OR Light Systems models that could fall in operating rooms. This hazard poses a risk of injury to surgical staff if the light system falls during use.
The light systems could fall from their mounting in the operating room due to design flaws. If the light falls, it may cause injury to staff or damage equipment.
Surgical staff and hospitals using the affected Maquet Orchide OR Light Systems models. Those with the specific model numbers and UDI-DI codes listed are most at risk.
Check your Maquet Orchide OR Light System model numbers and catalog numbers, which include OHDII FHD QL VP01, OHDII FHD QL AIR03, and other variants. Also look for the UDI-DI codes listed in the recall notice.
Identify your Maquet Orchide OR Light System model numbers and catalog numbers from the recall list.
Reach out to Getinge for assistance with the recall and to determine if your unit is affected.
The affected models include OHDII FHD QL VP01, OHDII FHD QL AIR03, and other variants with specific catalog numbers and UDI-DI codes listed in the recall notice.
Check your model numbers and catalog numbers against the list provided in the recall notice, which includes OHDII FHD QL VP01 and other variants with specific UDI-DI codes.
Contact Getinge directly to confirm if your unit is affected and follow their instructions for next steps.
We’ve drafted a message you can send Getinge to request your refund or repair — edit it as you like.
Subject: Recall Z-0762-2024 — Getinge Getinge Hello, I own a Getinge that is covered by recall Z-0762-2024 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.
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.
