FDA Device recall Z-2535-2019
Vanguard XP Tibial Tray 79 mm Item # 195252
- 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 79 mm Item # 195252 by Zimmer Biomet, citing the locking bar not fully engaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2535-2019 |
| 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 79 mm Item # 195252
Reason
The locking bar not fully engaging
Identifiers
| code_info | Lot Number 332750 833230 515120 752550 515130 373090 919280 754510 764430 764440 861230 837810 846560 907…Lot Number 332750 833230 515120 752550 515130 373090 919280 754510 764430 764440 861230 837810 846560 907730 928810 907720 907740 969000 969010 590620 590600 663320 663330 663340 590610 571010 663310 |
|---|
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-2535-2019%22
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