Zimmer Biomet, Inc. XP-CR Tibial Tray - Interlok 83 mm Item # 195277 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
XP-CR Tibial Tray - Interlok 83 mm Item # 195277
Brand
Zimmer Biomet, Inc.
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
Lot Number 141540 513160 571080 262460 938230 938260 966800 996040 066250 283280 663860 851390 663860R 090260 279290 376610 851380 663890 206880 374840 429310 723100 434300 469560 469560R 162000 258130 043950 320350 320330 076100 279070 600830 672690 599180 374130 576070 952400 450390 712610 717220 943430 141520 279280 376570 376590 513140
Zimmer Biomet, Inc. is recalling XP-CR Tibial Tray - Interlok 83 mm Item # 195277 due to The locking bar not fully engaging. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The locking bar not fully engaging
Recommended Action
Per FDA guidance
Risk 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 your recall records in the event of a compliance audit of your facilitys documentation. 5.If you have further questions or concerns after reviewing this notice, please call customer service at 574-371-3071 between 8:00 am and 5:00pm EST, Monday through Friday. Calls received outside of call center operating hours will receive a voicemail prompt or be transferred to an on-call representative in the event of an emergency. Alternatively, your questions may be emailed to CorporateQuality.PostMarket@zimmerbiomet.com. Surgeon Responsibilities: 1.Review this notification for awareness of the contents. 2.There are no specific patient monitoring instructions related to this recall that are recommended beyond your existing follow-up schedule. 3.A visual and audible confirmation should be made to ensure complete locking bar insertion. 4.Complete Attachment 1 Certificate of Acknowledgement and send to CorporateQuality.PostMarket@zimmerbiomet.com. 5.Retain a copy of the acknowledgement form with your recall records in the event of a compliance audit of your facilitys documentation. 6.If you have further questions or concerns after reviewing this notice, please call customer service at 574-371-3071 between 8:00 am and 5:00pm EST, Monday through Friday. Calls received outside of call center operating hours will receive a voicemail prompt or be transferred to an on-
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AL, AZ, AR, CA, CO, CT, FL, GA, ID, IL, IN, IA, KS, KY, LA, MD, MA, MI, MN, MS, MO, MT, NE, NV, NJ, NM, NY, NC, ND, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WV, WI, WY, DC
Page updated: Jan 10, 2026