FDA Device recall Z-2536-2019
Vanguard XP Tibial Tray 83 mm Item # 195253
- FDA Device
- Class II
- terminated
- Published 2019-09-18
On 2019-09-18 the FDA classified a Class II recall of Vanguard XP Tibial Tray 83 mm Item # 195253 by Zimmer Biomet, citing the locking bar not fully engaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2536-2019 |
| 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
Vanguard XP Tibial Tray 83 mm Item # 195253
Reason
The locking bar not fully engaging
Identifiers
| code_info | Lot Number 332760 752520 515140 754520 063070 072460 072440 072510 663350 663360 833240 919270 764460 846…Lot Number 332760 752520 515140 754520 063070 072460 072440 072510 663350 663360 833240 919270 764460 846570 764450 837820 861240 915690 915700 |
|---|
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-2536-2019%22
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