Device recall

Z-1012-05: Right Heart Catheter Product Line: Catalog Number 604315-------------406-1H-018…

FDA device recall · Class II · B. Braun Medical, Inc.

Key facts

Recall number (Z-number) Z-1012-05
Recall event 32177
Product Right Heart Catheter Product Line: Catalog Number 604315-------------406-1H-018 426D1009I18PP.
Product code DYG
Recalling firm B. Braun Medical, Inc.
Recall class Class II
Status Terminated
Termination date Dec 14, 2006
510(k) numbers K822806, K832287, K841639
FEI number 2523676

At a glance

  • 1–9 Linked 510(k)s
  • 10–99 Products in the same recall event
  • 10–99 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)