FDAApril 1, 2020device

PRESTIGE ATRAUMATIC GRASPER W/PORT DUAL ACTION, ROTATING 5mm DIAM., 36cm LENGTH. Product Code 8360-10

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

The hazard

Endoscopic graspers may become separated at the weld from handle to the shaft of the device.

What to do

FDA enforcement status: Completed

Brands named

aesculap implant systemsaesculapaesculap implant

UPCs

04046955083374

Recall history

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

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