FDA Device recall Z-2522-2019
XP-XP Tibial Tray - Interlok 71 mm Item # 195755
- 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 71 mm Item # 195755 by Zimmer Biomet, citing the locking bar not fully engaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2522-2019 |
| 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 71 mm Item # 195755
Reason
The locking bar not fully engaging
Identifiers
| code_info | Lot Number 450440 590880 512630 820720 820750 841600 841620 664320 841610 972770 589900 660500 664300 664…Lot Number 450440 590880 512630 820720 820750 841600 841620 664320 841610 972770 589900 660500 664300 664310 677650 841580 664300R 972750 998070 758320 044000 841590 044020 066160 677640 066150 381750 420270 664330 381750R 381730 433990 374560 282790 374540 420280 433960 381740 358960 758290 468150 505080 036280 998080 089890 358970 374570 499170 505060 358970R 374570R 322450 282800 499150 420250 499160 499180 592370 468140 505070 592380 592350 322460 036270 505050 840730 885090 840710 855340 864720 885080 592360 592400 916860 958440 916850 828720 975610 958430 011470 023380 061400 061410 984770 181440 103040 181420 103030 131230 159310 061420 116010 116030 261080 293870 241450 297200 336140 293850 223150 241440 261090 384230 336980 337000 093400 223130 201950 297070 371590 336130 556580 587300 371560 418730 432380 384220 467200 511470 599810 599810R 634230 664180 |
|---|
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-2522-2019%22
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