FDA Device recall Z-2517-2019
XP-XP Tibial Tray - Interlok 87 mm Item # 195760
- 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 87 mm Item # 195760 by Zimmer Biomet, citing the locking bar not fully engaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2517-2019 |
| 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 87 mm Item # 195760
Reason
The locking bar not fully engaging
Identifiers
| code_info | Lot Number 790970 984810 984820 202000R 664250R 664280R 685040 885800 716010 873630 903460 960480 960500…Lot Number 790970 984810 984820 202000R 664250R 664280R 685040 885800 716010 873630 903460 960480 960500 201990 202000 664250 664280 400690 394670 394710 293220 183680 394330 |
|---|
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-2517-2019%22
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