Device recall

Z-1883-2009: Pyxis Anesthesia System 3500, Cardinal Health, Clinical Technologies and…

FDA device recall · Class II · Cardinal Health Manufacturing LLC

Key facts

Recall number (Z-number) Z-1883-2009
Recall event 52767
Product Pyxis Anesthesia System 3500, Cardinal Health, Clinical Technologies and Services, San Diego, CA. The Pyxis Anesthesia Station 3500 is a medication dispensing product that provides medication and inventory management for the anesthesiologist at the point of care within the operating room. The system…
Product code BRY
Recalling firm Cardinal Health Manufacturing LLC
Recall class Class II
Status Terminated
Termination date Mar 28, 2012
FEI number 3003879246

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)