Device recall

Z-0401-2010: Power Circular Stapler 21 mm Digital Loading Unit, product code PCS21; Power…

FDA device recall · Class II · Surgical Devices/Covidien

Key facts

Recall number (Z-number) Z-0401-2010
Recall event 53694
Product Power Circular Stapler 21 mm Digital Loading Unit, product code PCS21; Power Circular Stapler 29 mm Digital Loading Unit, product code PCS29.
Product code GDW
Recalling firm Surgical Devices/Covidien
Recall class Class II
Status Terminated
Termination date Mar 8, 2010
510(k) numbers K040024
FEI number 1219930

At a glance

  • 1–9 Linked 510(k)s
  • 10–99 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)