FDA Device recall Z-2531-2019
Vanguard XP Tibial Tray 69 mm Item # 195248
- 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 69 mm Item # 195248 by Zimmer Biomet, citing the locking bar not fully engaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2531-2019 |
| 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 69 mm Item # 195248
Reason
The locking bar not fully engaging
Identifiers
| code_info | Lot Number 117720 332660 373010 373000 514970 515000 372990 039210 112980 113000 112990 202920 303370 303…Lot Number 117720 332660 373010 373000 514970 515000 372990 039210 112980 113000 112990 202920 303370 303380 590480 660400 660410 584210 590490 833180 752040 752050 752560 752060 919220 928860 754470 764360 837750 764350 846490 861180 881480 881490 928870 846500 881460 984370 984380 984360 837760 570940 |
|---|
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-2531-2019%22
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