FDA Device recall Z-2520-2019
XP-XP Tibial Tray - Interlok 75 mm Item # 195757
- 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 75 mm Item # 195757 by Zimmer Biomet, citing the locking bar not fully engaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2520-2019 |
| 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 75 mm Item # 195757
Reason
The locking bar not fully engaging
Identifiers
| code_info | Lot Number 664400 664380 677580 562210 758380 650470 677760 677590 677750 758410 664390 664410 677570 613…Lot Number 664400 664380 677580 562210 758380 650470 677760 677590 677750 758410 664390 664410 677570 613450 972810 972820 998120 158870 677770 677780 998110 283010 273090 273100 677740 703240 592490 592490R 592530 592620 703080 592660 703160 703160R 558590 592640 592650 592640R 558580 703090 703120 282950 505130 505140 703100 703190 703230 703260 703200 158890 283020 558570 592510 592520 592630 677720 703070 703170 703210 791010 592520R 322550 322530 592500 885120 975630 505160 864740 958470 855430 592540 703150 828740 505150 703060 703130 703140 703060R 840750 103060 131250 159330 131250R 011490 061450 093420 181470 703180 023400 116070 201970 036310 336740 241480 223190 261110 297090 371620 371640 384280 418750 432410 634300 599880 556600 664220 467240 511490 715900 715910 587370 684980 716120 920620 882120 906770 029290 906760 986000 072990 986030 396430 126060 |
|---|
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-2520-2019%22
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