ClearanceBrief
Recall Z-2516-2021 ยท HRY Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer

Aesculap Implant Systems LLC

Univation X System Tray Sysem knee implant devices as follows: Tray Number/Set Name/Set Number NM1090R Navigation Set ST0560; NM1092R + NM1095R + NM1096R (Tray insert to NM1095R) univation XF ST0540; NM1093R univation XF OPT ST0544

DateMar 19, 2021
StatusTerminated
ReasonMalfunction- loosening of the implant resulting in a potential revision surgery
Root causeUnknown/Undetermined by firm
ActionAesulap issued An Urgent Medical Device Recall via USPS overnight to consignees on March 19, 2021. Letter states reason for recall, health risk and action to take: Immediately examine your inventory, identify and quarantine product related to this notification. In addition, if you have further distributed this product, please identify your customers and notify them at once of this Recall Notification. Your notification to your customers may be enhanced by including a copy of this notification letter. A representative of Aesculap will reach out to you to assist in the return of affected produc
DistributionUS Nationwide distribution.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K081293UNIVATION UNICONDYLAR KNEE SYSTEM
Aesculap Implant Systems, Inc., Sep 22, 2008
K131167UNIVATION
Aesculap Implant Systems, LLC, Oct 17, 2013