FDA Device recall Z-2529-2019
Vanguard XP Tibial Tray 65 mm Item # 195246
- 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 65 mm Item # 195246 by Zimmer Biomet, citing the locking bar not fully engaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2529-2019 |
| 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 65 mm Item # 195246
Reason
The locking bar not fully engaging
Identifiers
| code_info | Lot Number 833150 332620 514900 752000 372950 752010 919200 837730 764310 764320 884350 883500 968960 968…Lot Number 833150 332620 514900 752000 372950 752010 919200 837730 764310 764320 884350 883500 968960 968970 968980 754450 883450 584190 861150 660380 |
|---|
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-2529-2019%22
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