FDA Device recall Z-2519-2019
XP-XP Tibial Tray - Interlok 79 mm Item # 195758
- 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 79 mm Item # 195758 by Zimmer Biomet, citing the locking bar not fully engaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2519-2019 |
| 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 79 mm Item # 195758
Reason
The locking bar not fully engaging
Identifiers
| code_info | Lot Number 664420 664430 677600 677610 219880 841630 158920 158940 758430 758450 102010 972850 998140 089…Lot Number 664420 664430 677600 677610 219880 841630 158920 158940 758430 758450 102010 972850 998140 089940 998150 101990 101980 273110 972840 036320 283060 322560 273120 273120R 322570 592590 592600 592550 703470 703530 703480 703540 703580 592560 703450 703490 703510 703570 703590 703500 703520 592610 703550 283040 592580 703460 790990 102000 592570 703600 791020 828750 703610 966270 061470 093430 703620 975640 011500 023410 061460 093440 703560 855460 864750 131260 116090 103070 241490 181480 201980 223200 159340 885130 336760 090000 297100 371660 467260 418760 371670 432440 556610 261120 585790 384310 511500 587390 634320 530660 384300 664230 685000 715980 882150 715960 906780 906800 920630 715970 126070 126080 073010 029300 396490 986060 163050 986090 221460 247420 163070 247410 293180 293190 318620 374550 374560 318600 442030 390200 390220 442020 478600 509 |
|---|
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-2519-2019%22
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