DKK Dai-Ichi Shomei recalls Aurora 3 and 7 lighthead models (AUT7) due to potential weld cracks causing frame sagging 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 3 Series and Aurora 7 lighthead models (AUT7) because a weld crack could cause the light head frame to sag, crack the plastic housing, or detach. This poses a risk during surgical procedures where the light is critical for visibility.
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 the light's stability during surgery, potentially affecting the surgical field visibility.
Surgical staff and hospitals that own or use Aurora 3 Series or Aurora 7 lighthead models (AUT7) with serial numbers listed in the recall. The risk is highest for users during surgical procedures where the light head is critical for visibility.
Check if your Aurora 3 Series or Aurora 7 lighthead has a model number starting with AUT7 (including TV models). Serial numbers listed in the recall include a range from 13040011 to 14080303.
Look for the serial number on your lighthead, which should be in the range 13040011 to 14080303 as listed in the recall.
Aurora 3 Series and Aurora 7 lighthead models with serial numbers from 13040011 to 14080303 (specifically model AUT7).
The weld on the light head frame can crack, causing the frame to sag, the plastic housing to crack, or the light head to detach during surgery, which could compromise visibility of the surgical site.
Yes, check if your lighthead has a serial number in the range 13040011 to 14080303. If it does, contact the manufacturer for further instructions.
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-2620-2024 — DKK Dai-Ichi Shomei DKK Dai-Ichi Shomei Hello, I own a DKK Dai-Ichi Shomei that is covered by recall Z-2620-2024 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.
