XP-XP Tibial Tray — Class II medical device recall Z-2519-2019
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-2519-2019 |
|---|---|
| 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 |
| Lot numbers | 011500, 018220, 018260, 023410, 029300, 036320, 061460, 061470, 073010, 076760, 076770, 089940, 090000, 093430, 093440, 101980, 101990, 102000, 102010, 103070, 111740, 111760, 116090, 126070, 126080, 131260, 137540, 158920, 158940, 159340, 163050, 163070, 181480, 183560, 191200, 201980, 219880, 221460, 223200, 241490 and 130 more |
| Model numbers | 195758 |
Product
XP-XP Tibial Tray - Interlok 79 mm Item # 195758
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-2519-2019. 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.