Aesculap Implant Systems LLC recalls PRESTIGE ATRAUMATIC GRASPER W/PORT DUAL ACTION, ROTATING 5mm
Recalled Product
PRESTIGE ATRAUMATIC GRASPER W/PORT DUAL ACTION, ROTATING 5mm DIAM., 36cm LENGTH. Product Code 8360-10
Hazard / Issue
Endoscopic graspers may become separated at the weld from handle to the shaft of the device.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: UDI-DI: 04046955083374, lots M45041; M45399; M45711; M46069; M46350; M47462; M47893; M48115; M48279; M48346; M48467; M48596; M48753; M48848; M48907; M49375; M49435; M49632; M49683; M49711; M49867; M55796.
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