Device recall

Z-1828-2026: CUSA Clarity C7000 Console, Software Version: 2.1.1.909. Ultrasonic surgical…

FDA device recall · Class II · Integra LifeSciences Corp. (NeuroSciences)

Key facts

Recall number (Z-number) Z-1828-2026
Recall event 98476
Product CUSA Clarity C7000 Console, Software Version: 2.1.1.909. Ultrasonic surgical aspirator system.
Product code LFL
Recalling firm Integra LifeSciences Corp. (NeuroSciences)
Recall class Class II
Status Open, Classified
510(k) numbers K161882
FEI number 3003418325

At a glance

  • 1–9 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)