RecallRadar

FDA Device recall Z-2506-2019

XP-CR Tibial Tray - Interlok 67mm Item # 195271

On 2019-09-18 the FDA classified a Class II recall of XP-CR Tibial Tray - Interlok 67mm Item # 195271 by Zimmer Biomet, citing the locking bar not fully engaging.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2506-2019
ClassificationClass II
Statusterminated
Initiated2019-08-15
Published2019-09-18
Last updated2026-09-13 11:55 UTC
CompanyZimmer Biomet
DistributionAL, AR, AZ, CA, CO, CT, DC, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WI, WV, WY

Product

XP-CR Tibial Tray - Interlok 67mm Item # 195271

Reason

The locking bar not fully engaging

Identifiers

code_info
Lot Number 486100 262400 291180 584260 663550 562250 666830 660450 841520 917700 966720 966720R 075450 07…Lot Number 486100 262400 291180 584260 663550 562250 666830 660450 841520 917700 966720 966720R 075450 075460 075500 663530 995960 322020 043860 090190 206820 075440 745670 352820 383680 075470 745650 513340 159230 258060 429230 161960 161950 161930 161910 161920 162010 161860 274480 161870 161900 274460 996070 274490 274510 721690 322000 456750 456750R 274470 374780 951150 075510 469490 721670 309710 274500 309680 309690 075490 309700 585540 883560 221140 374030 920540 279010 450330 672510 575980 821280 943360 599120 600770 712550 717160 017970 076400 076410 220040 175290 175290R 289160 676270 676300 228610 351290 395400 395420 445370 395400R

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2506-2019%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.