Zimmer Biomet, Inc. XP-CR Tibial Tray - Interlok 71mm Item # 195273 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
XP-CR Tibial Tray - Interlok 71mm Item # 195273
Brand
Zimmer Biomet, Inc.
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
Lot Number 663640 262420 571030 590700 590710 676280 917650 320580 966740 995980 996090 966740R 043890 159270 206840 258080 283210 841530 043900 066200 090220 066200R 322070 322070R 383700 352840 283180 359640 322090 429260 374800 403830 159260 456770 041150 579240 899740 274590 274530 274580 041240 041190 503440 585580 993810 666890 503460 888430 221170 985320 374080 374070 279030 599140 576020 943390 821310 411240 450350 600790 712570 717180 717180R 018020 111590 676310 676310R 072520 218650 291200 072520R 672570 289190 562280 148430 291190 351320 445400 445410 486120 445400R 445410R
Zimmer Biomet, Inc. is recalling XP-CR Tibial Tray - Interlok 71mm Item # 195273 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