Aesculap Implant Systems LLC recalls PRESTIGE RETRACTION GRASPER, W/PORT DUAL ACTION, ROTATING 5m
Recalled Product
PRESTIGE RETRACTION GRASPER, W/PORT DUAL ACTION, ROTATING 5mm DIAM., 36cm LENGTH. Product Code 8361-10
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: 04046955083381, lots M45171; M46651; M47463; M48124; M49436.
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