Class II — DKK Dai-Ichi Shomei Co., Ltd.
| Recalling firm | DKK DAI-ICHI SHOMEI CO, LTD |
|---|---|
| Registered facility | DKK DAI-ICHI SHOMEI CO, LTD (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | 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. |
| Product | LFS Flat screen support arm systems without surgical lamp for models Aurora series, Aurora 2 series, Aurora 3 series, Aurora 4 series, Aurora Astro series, Stellar XL, and Stellar series, LFS Flat Screen Support Arm Model Numbers |
| Quantity | 1211 units |
| Distribution | US States: MI |
| Initiated | 2023-08-23 |
| Classified | 2023-10-05 |
| Recall number | Z-0072-2024 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — DKK Dai-Ichi Shomei Co., Ltd. (Z-0072-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/92999/
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