FDA Device recall Z-2523-2019
XP-XP Tibial Tray - Interlok 69 mm Item # 195754
- 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 69 mm Item # 195754 by Zimmer Biomet, citing the locking bar not fully engaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2523-2019 |
| 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 69 mm Item # 195754
Reason
The locking bar not fully engaging
Identifiers
| code_info | Lot Number 590860 660490 590850 560350 562180 650420 758270 841570 650430 613370 303400 589890 972740 998…Lot Number 590860 660490 590850 560350 562180 650420 758270 841570 650430 613370 303400 589890 972740 998060 998040 972730 043990 066130 101900 174980 282760 101920 174970 207000 258020 101920R 066140 101890 101930 258030 036260 322420 374530 374550 358950 358950R 036250 358940 207020 336660 207010 420360 336960 558600 558610 592310 374520 420400 592340 282770 592330 499140 499130 499130R 381700 381710 499110 322400 381720 802050 855300 802050R 802060 840700 864710 802060R 061380 223100 885070 958400 975590 975600 011450 023370 958410 984760 011440 499120 828710 166070 885060 916840 916840R 840690 558620 061390 115970 131220 115990 159300 181400 093390 181410 201940 103020 293790 223090 297190 293820 592290 418710 336120 418700 336100 418690 420380 467190 599780 511460 556570 634200 664170 705610 684910 587280 684900 297180 716090 705630 716080 715810 715790 882080 |
|---|
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-2523-2019%22
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