ClearanceBrief
Recall Z-2520-2019 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Zimmer Biomet, Inc.

XP-XP Tibial Tray - Interlok 75 mm Item # 195757

DateAug 15, 2019
StatusTerminated
ReasonThe locking bar not fully engaging
Root causeManufacturing material removal
ActionRisk Manager Responsibilities: 1.Review this notification and ensure that affected personnel are aware of the contents. 2.If you have affected product at your facility, assist your Zimmer Biomet sales representative and quarantine all affected product. Your Zimmer Biomet sales representative will remove the affected product from your facility. 3.Complete Attachment 1 Certificate of Acknowledgement and send to CorporateQuality.PostMarket@zimmerbiomet.com. This form will be returned even if you do not have affected products at your facility. 4.Retain a copy of the acknowledgement form with
Quantity973 units
DistributionState NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K132873VANGUARD XP KNEE SYSTEM
Biomet, Inc., Dec 11, 2013