Device recall

Z-1464-2013: da Vinci 5 mm Flared Instrument Cannulae for use with the da Vinci S and Si…

FDA device recall · Class II · Intuitive Surgical, Inc.

Key facts

Recall number (Z-number) Z-1464-2013
Recall event 65168
Product da Vinci 5 mm Flared Instrument Cannulae for use with the da Vinci S and Si Surgical Systems. Used to establish a port of entry for Intuitive Surgical EndoWrist instruments
Product code NAY
Recalling firm Intuitive Surgical, Inc.
Recall class Class II
Status Terminated
Termination date Apr 15, 2014
FEI number 3001675293

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)