FDAJune 12, 2023device

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

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

The hazard

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.

What to do

FDA enforcement status: Ongoing

Brands named

intuitive surgicalintuitive

UPCs

00886874112496

Recall history

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

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