Device recall

Z-1244-2007: Endoscopic Instrument Control System (da Vinci Surgical System) Model IS1200…

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

Key facts

Recall number (Z-number) Z-1244-2007
Recall event 38069
Product Endoscopic Instrument Control System (da Vinci Surgical System) Model IS1200, A4.3 SW level, Manufactured by Intuitive Surgical, Inc, Sunnyvale, CA 94086
Product code NAY
Recalling firm Intuitive Surgical, Inc.
Recall class Class II
Status Terminated
Termination date Jul 2, 2008
510(k) numbers K021036, K990144
FEI number 3001675293

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

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