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Serious recall: Injury is possible or has been reported. Take action promptly.

Intuitive Surgical, Inc. 2026-01-21 Health serious FDA
Health · FDA · Recall #FDA-Z-1096-2026

da Vinci SP, SP Access Port Kit, Large Incision Reference Numbers:430073… Recall

Issued January 21, 2026 · Intuitive Surgical, Inc.

In January 2026, Intuitive Surgical, Inc. recalled the da Vinci SP, SP Access Port Kit, Large Incision Reference Numbers:430073…, a serious health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

Access Port System tray may develop cracks potentially resulting in a sterility breach.

What you should do

  1. 1 Stop using da Vinci SP, SP Access Port Kit, Large Incision Reference Numbers:430073… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Intuitive Surgical, Inc. to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Intuitive Surgical, Inc.
Category
Health
Recall date
January 21, 2026
Units affected
Not reported
Sold at
Worldwide - US Nationwide distribution including in the states of Alabama, Arizona, California, Colorado, Connecticut, Florida, Georgia, Ill
Recall number
FDA-Z-1096-2026
Made in
United States
Issuing agency
FDA

In context

  • Intuitive Surgical, Inc. has 11 recalls in our database.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 356th Health recall we've logged in 2026.
Read the official FDA notice

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