Device recall

Z-2465-2010: Spider Flex Monopolar Hook (Spider Surgical Instruments), TransEnterix, Inc…

FDA device recall · Class II · Transenterix, INC

Key facts

Recall number (Z-number) Z-2465-2010
Recall event 56179
Product Spider Flex Monopolar Hook (Spider Surgical Instruments), TransEnterix, Inc., Durham, NC
Product code GCJ
Recalling firm Transenterix, INC
Recall class Class II
Status Terminated
Termination date Jan 31, 2011
510(k) numbers K091697
FEI number 3007593944

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)