FDAMarch 17, 2022device

da Vinici X da Vinci Xi Sureform 45 REF 480445 da Vinci X da Vinci Xi Sureform 45 Curved-Tip REF 480545 da Vinici X da Vinci Xi Sureform 60 REF 480460

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

As a result of complaint data review, it identified tissue pushout events occurring during firing of the SureForm stapler when tissue is pushed distally within the jaws, rather than being held in place and transected. Overall rate of harm associated with bleeding of critical severity exceeds the predicted likelihood of harm as documented within Intuitives existing risk documentation.

What to do

FDA enforcement status: Ongoing

Brands named

intuitive surgicalintuitive

UPCs

008868741175830088687411759000886874115640

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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da Vinici X da Vinci Xi Sureform 45 REF 480445 da Vinci X da Vinci Xi Sureform 45 Curved-Tip REF 480545 da Vinici X da Vinci Xi Sureform 60 REF 480460 — Recall Details · AllClear