# FDA recall Z-0072-2024

> **DKK Dai-Ichi Shomei Co., Ltd.** · Class II · device recall initiated 2023-08-23.

## 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

## Reason for recall

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.

## Distribution

US States: MI

## Key facts

- **Recall number:** Z-0072-2024
- **Recalling firm:** DKK Dai-Ichi Shomei Co., Ltd.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-08-23
- **Report date:** 2023-10-11

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Itabashi, N/A, Japan

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0072-2024

## Citation

> AI Analytics. FDA recall Z-0072-2024. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0072-2024. Source: US FDA. Licensed CC0.

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