Reported Jul 12, 2023 · Ongoing

da Vinci Xi/X Tip-Up Fenestrated Grasper, REF: 470347, VER: 12

Intuitive Surgical, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Intuitive Surgical, Inc. · 1266 Kifer Rd Bldg 101 · Sunnyvale, CA · 94086-5304

Is this the product you have?

  • da Vinci Xi/X Tip-Up Fenestrated Grasper
  • REF470347
  • VER12
Lot codes and dates
  • UDI-DI00886874112496, All Lots
Amount recalled
46,033

Where it was sold

Why it was recalled

Fenestrated Graspers have a manufacturing issue has the potential to cause breakage on both upper and/or lower grips, which could lead to stainless steel fragments falling into the patient that may be either detected or undetected.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:57 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.