FDA Device recall Z-2521-2019
XP-XP Tibial Tray - Interlok 73 mm Item # 195756
- FDA Device
- Class II
- terminated
- Published 2019-09-18
On 2019-09-18 the FDA classified a Class II recall of XP-XP Tibial Tray - Interlok 73 mm Item # 195756 by Zimmer Biomet, citing the locking bar not fully engaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2521-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-08-15 |
| Published | 2019-09-18 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Zimmer Biomet |
| Distribution | AL, 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-XP Tibial Tray - Interlok 73 mm Item # 195756
Reason
The locking bar not fully engaging
Identifiers
| code_info | Lot Number 562200 664340 613420 512640 820800 820820 650460 422530 820780 677550 589910 664350 664360 664…Lot Number 562200 664340 613420 512640 820800 820820 650460 422530 820780 677550 589910 664350 664360 664370 677540 677560 972780 758360 758340 972800 089920 101940 158830 273080 158830R 101950 158840 207050 101960 036290 036300 322490 998100 282810 322510 358980 434000 434000R 282840 434050 101970 207040 358990 468160 499260 505110 468170 505120 499270 499270R 558560 558540 273050 505100 558550 282880 207030 434010 499280 864730 885110 592460 916870 791000 916880 592480 828730 885100 434040 592470 505090 840740 061430 061440 499290 975620 093410 958450 011480 103050 159320 223170 261100 293920 293890 293910 297080 131240 181450 181460 201960 241470 855400 337030 336160 371610 384240 998090 371600 116050 432340 592450 023390 336150 384260 511480 418740 599840 556590 634270 467220 664210 716110 684960 705680 715890 587340 920610 985960 882110 906750 906740 985980 0 |
|---|
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-2521-2019%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.