DKK Dai-Ichi Shomei recalls LFS Flat Screen Arm Systems with surgical lamps for Aurora and Stellar series due to risk of spring shaft breakage from missing stopper blocks.
The stopper block on the LFS bracket could be broken or missing. Without this stopper block, the flat screen attached to the LFS flat screen system can rotate beyond the original angle limit and it could cause excessive force to be given to the spring shaft of the LFS bracket. Due to the excessive force given to the spring shaft, the spring shaft could break and shear off.
DKK Dai-Ichi Shomei is recalling LFS Flat Screen Arm Systems with surgical lamps for Aurora and Stellar series models. The stopper block could be broken or missing, causing the screen to rotate too far and potentially breaking the spring shaft.
The stopper block on the LFS bracket could be broken or missing. Without this stopper block, the flat screen can rotate beyond its original angle limit, creating excessive force on the spring shaft. This excessive force can cause the spring shaft to break and shear off.
Surgical staff and medical facilities using the LFS Flat Screen Arm Systems with surgical lamps for Aurora, Aurora 2, Aurora 3, Aurora 4, Stellar XL, and Stellar series models are most at risk.
Check for LFS Flat Screen Arm System models labeled Aurora, Aurora 2, Aurora 3, Aurora 4, Stellar XL, or Stellar series. Look for specific model numbers and serial numbers listed in the recall notice.
Inspect the LFS bracket for a broken or missing stopper block.
If the stopper block is broken or missing, stop using the system immediately.
Aurora, Aurora 2, Aurora 3, Aurora 4, Stellar XL, and Stellar series models with specific model numbers and serial numbers listed in the recall notice.
Stop using the system immediately if the stopper block is broken or missing.
The recall does not specify a fix; the remedy is null.
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-0071-2024 — DKK Dai-Ichi Shomei DKK Dai-Ichi Shomei Hello, I own a DKK Dai-Ichi Shomei that is covered by recall Z-0071-2024 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.
