Product Safety Recalls

Product Recall Tracker

Aesculap Implant Systems LLC Recall 90493

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

Aesculap Implant Systems LLC Recall 90493 Information

StatusCompleted
Mandated?Voluntary: Firm initiated
Recall NumberZ-1481-2022
Event ID90493
Event DescriptionPRESTIGE ATRAUMATIC GRASPER W/PORT DUAL ACTION, ROTATING 5mm DIAM., 36cm LENGTH. Product Code 8360-10
Product TypeDevices
DistributionUnited 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.
Quantity3392
Recall ReasonEndoscopic graspers may become separated at the weld from handle to the shaft of the device.
Device Classification20220810
Device Code InfoUDI-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.
Center Classification Date20220729
Recall Initiation Date20200401
Recalling FirmAesculap Implant Systems LLC
Initial Notification Letter
Similar To

© 2021 Recall.Report / Contact / Privacy Policy

This site's data is aggregated programmatically and provided "as is" without any representations or warranties, express or implied.
Recall.report is not affiliated with the Consumer Product Safety Commision, FDA, or US government in any way.