FDA Device recall Z-2504-2019
XP-CR Tibial Tray - Interlok 63mm Item # 195269
- FDA Device
- Class II
- terminated
- Published 2019-09-18
On 2019-09-18 the FDA classified a Class II recall of XP-CR Tibial Tray - Interlok 63mm Item # 195269 by Zimmer Biomet, citing the locking bar not fully engaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2504-2019 |
| 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-CR Tibial Tray - Interlok 63mm Item # 195269
Reason
The locking bar not fully engaging
Identifiers
| code_info | Lot Number 663420 993820 660430 660430R 262380 395340 445350 584240 562230 578990 579070 043840 159200 91…Lot Number 663420 993820 660430 660430R 262380 395340 445350 584240 562230 578990 579070 043840 159200 917670 996050 043840R 917670R 206800 090150 159210 352790 995940 352780 469480 321920 663450 258040 352770 966700 434250 434260 456730 274630 374760 672430 899750 041270 899710 041200 666860 278990 600750 712530 600750R 821250 821250R 450310 599050 599050R 199780 717140 943340 017920 076390 220020 220020R 175270 228580 175270R 199790 199790R 395350 |
|---|
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-2504-2019%22
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