Aesculap Implant Systems LLC: Medical Device Recall in 2022 - (Recall #: Z-1481-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: April 1, 2020

Date Posted: August 10, 2022

Recall Number: Z-1481-2022

Event ID: 90493

Reason for Recall:

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

Status: Completed

Product Quantity: 3392

Code Information:

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.

Distribution Pattern:

United States Nationwide distribution in the states of AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV, WY, Washington DC and Puerto Rico.

Voluntary or Mandated:

Voluntary: Firm initiated