FDA Device recall Z-2533-2019
Vanguard XP Tibial Tray 73 mm Item # 195250
- 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 73 mm Item # 195250 by Zimmer Biomet, citing the locking bar not fully engaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2533-2019 |
| 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 73 mm Item # 195250
Reason
The locking bar not fully engaging
Identifiers
| code_info | Lot Number 590540 590530 590520 663190 590550 663200 907710 117740 332690 833210 752580 373050 373060 515…Lot Number 590540 590530 590520 663190 590550 663200 907710 117740 332690 833210 752580 373050 373060 515050 752120 515070 752100 752110 754490 764390 861210 837790 936210 764400 846520 928890 907690 936220 936230 954050 928880 936200 954030 907700 063000 062990 570980 584230 |
|---|
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-2533-2019%22
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