FDA Device recall Z-2512-2019
XP-CR Tibial Tray - Interlok 83 mm Item # 195277
- 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 83 mm Item # 195277 by Zimmer Biomet, citing the locking bar not fully engaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2512-2019 |
| 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 83 mm Item # 195277
Reason
The locking bar not fully engaging
Identifiers
| code_info | Lot Number 141540 513160 571080 262460 938230 938260 966800 996040 066250 283280 663860 851390 663860R 09…Lot Number 141540 513160 571080 262460 938230 938260 966800 996040 066250 283280 663860 851390 663860R 090260 279290 376610 851380 663890 206880 374840 429310 723100 434300 469560 469560R 162000 258130 043950 320350 320330 076100 279070 600830 672690 599180 374130 576070 952400 450390 712610 717220 943430 141520 279280 376570 376590 513140 |
|---|
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-2512-2019%22
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