FDAMarch 3, 2022device

VESSEL SEALER EXTEND, Single-Use Instrument EndoWrist Instruments 8mm, da Vinci X' da Vinci Xi', REF 480422

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

00886874115664

Recall history

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

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