FDAMarch 3, 2022device

DAVINCI | Energy SynchroSeal da Vinci X' da Vinci Xi', Single Use Instrument 8mm, REF 480440

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

The hazard

Placing excessive tissue in the instrument jaws of the devices prior to sealing and transection can result in an insufficient seal.

What to do

FDA enforcement status: Ongoing

Brands named

intuitive surgicalintuitive

UPCs

00886874117309

Recall history

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

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