FDA Device recall Z-2524-2019
XP-XP Tibial Tray - Interlok 67 mm Item # 195753
- 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 67 mm Item # 195753 by Zimmer Biomet, citing the locking bar not fully engaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2524-2019 |
| 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 67 mm Item # 195753
Reason
The locking bar not fully engaging
Identifiers
| code_info | Lot Number 562170 613350 677700 677680 664240 758250 758230 753770 753780 998030 753790 590830 590840 660…Lot Number 562170 613350 677700 677680 664240 758250 758230 753770 753780 998030 753790 590830 590840 660470 660480 664230 664260 664270 677660 677670 677710 590830R 677660R 677670R 972690 758210 972710 206980 174950 174950R 174960 206970 258000 258010 664290 664290R 664280 206960 282720 322360 468220 036240 219760 336620 359230 358920 592270 336640 592260 592260R 592230 592240 592250 592220 282740 322380 468230 358930 864700 802030 885040 802030R 802020 828700 828700R 975580 958380 840680 855270 011430 023360 061360 592200 916830 131190 093380 201930 223080 241430 103010 181390 159290 984750 297170 115960 261150 293750 958370 261160 336090 418680 432510 061340 587260 511450 599740 705580 634170 705560 664160 684880 715770 715750 716070 715760 716050 882070 985900 029240 906680 920570 029230 125980 396320 221370 072850 162930 162950 247270 247300 293090 318450 3184 |
|---|
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-2524-2019%22
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