DKK Dai-Ichi Shomei recalls Aurora 4 and 7 lighthead models (AUA7) due to potential weld cracks causing frame sagging, housing cracks, or detachment during surgery.
The weld on the light head frame can crack which could lead to problems such as the light head frame sagging, the plastic front face housing cracking, or the light head detaching.
DKK Dai-Ichi Shomei is recalling Aurora 4 Series and Aurora 7 lighthead surgical lights because a weld on the light head frame can crack. This could cause the frame to sag, the plastic housing to crack, or the light head to detach during surgery, potentially affecting surgical safety.
The weld on the light head frame can crack over time, which may cause the frame to sag, the plastic front housing to crack, or the entire light head to detach from the surgical instrument. This could compromise surgical visibility and safety during procedures.
Surgical staff and hospitals that own or use Aurora 4 Series or Aurora 7 lighthead models (AUA7) with serial numbers listed in the recall. The risk is highest for users during surgical procedures.
Check for Aurora 4 Series or Aurora 7 lighthead models with serial numbers listed in the recall (e.g., 07120133, 2015-03-0001 through 2023-11-0555). The product is used in surgical settings to illuminate the operating field.
Verify if your Aurora 4 Series or Aurora 7 lighthead has a serial number listed in the recall (e.g., 07120133, 2015-03-0001 through 2023-11-0555).
If your product is affected, contact DKK Dai-Ichi Shomei for further instructions on potential remedies.
The recalled models are Aurora 4 Series and Aurora 7 lighthead with serial numbers listed in the recall (e.g., 07120133, 2015-03-0001 through 2023-11-0555).
The weld on the light head frame can crack over time, potentially causing the frame to sag, the plastic housing to crack, or the light head to detach during surgery.
No, but you should check if your product is affected and contact the manufacturer for guidance if it is.
We’ve drafted a message you can send DKK Dai-Ichi Shomei to request your refund or repair — edit it as you like.
Subject: Recall Z-2621-2024 — DKK Dai-Ichi Shomei DKK Dai-Ichi Shomei Hello, I own a DKK Dai-Ichi Shomei that is covered by recall Z-2621-2024 from DKK Dai-Ichi Shomei. 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.
