FDA Device recall Z-2530-2019
Vanguard XP Tibial Tray 67 mm Item # 195247
- 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 67 mm Item # 195247 by Zimmer Biomet, citing the locking bar not fully engaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2530-2019 |
| 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 67 mm Item # 195247
Reason
The locking bar not fully engaging
Identifiers
| code_info | Lot Number 332640 833160 514940 372960 372970 514920 752020 752030 919210 764330 754460 884550 837740 764…Lot Number 332640 833160 514940 372960 372970 514920 752020 752030 919210 764330 754460 884550 837740 764340 861170 884360 887950 935780 935800 953910 968990 953950 928850 936190 953930 953940 861160 663120 660390 663080 663110 584200 |
|---|
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-2530-2019%22
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