Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0071-2024 — LFS Flat screen arm system with 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 Arm System Model Numbers LFSST2323, LFSLFSST29TV23, LFSST29TV23, LFSST23TV, LFSST23, LFSST2323TV, LFSLFSST23

U.S. FDA — Device Enforcement · Japan · 2023-08-23 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0071-2024
Date of alert
2023-08-23
Country / jurisdiction
Japan
Risk level
Class II
Risk type
recall
Brand
DKK Dai-Ichi Shomei Co., Ltd.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
06087323
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.