Device recall

Z-0072-2024: LFS Flat screen support arm systems without surgical lamp for models Aurora…

FDA device recall · Class II · DKK Dai-Ichi Shomei Co., Ltd.

Key facts

Recall number (Z-number) Z-0072-2024
Recall event 92999
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
Product code FSY
Recalling firm DKK Dai-Ichi Shomei Co., Ltd.
Recall class Class II
Status Open, Classified
FEI number 3006437518

At a glance

  • None Linked 510(k)s
  • 1–9 Products in the same recall event
  • 100–999 Recalled products with this product code

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device recalls (products)

Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.

Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database

Browse all FDA device recalls (products)