Vanguard XP Tibial Tray 73 mm Item # 195250 — Class II medical device recall Z-2533-2019
Terminated recall by Zimmer Biomet, Inc., reported 2019-09-18, distributed in AL, AR, AZ, CA, CO, CT, DC, FL…. The locking bar not fully engaging
| Recall number | Z-2533-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2019-08-15 |
| Classified | 2019-09-12 |
| Reported by FDA | 2019-09-18 |
| Terminated | 2021-04-16 |
| Distributed | 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 |
| Countries outside the US | AU, CA, CN, IT, JP, KR, SE |
| Quantity | 84 units |
| Lot numbers | 062990, 063000, 117740, 332690, 373050, 373060, 515050, 515070, 570980, 584230, 590520, 590530, 590540, 590550, 663190, 663200, 752100, 752110, 752120, 752580, 754490, 764390, 764400, 833210, 837790, 846520, 861210, 907690, 907700, 907710, 928880, 928890, 936200, 936210, 936220, 936230, 954030, 954050 |
| Model numbers | 195250 |
Product
Vanguard XP Tibial Tray 73 mm Item # 195250
Reason for recall
The locking bar not fully engaging
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2533-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.