XP-XP Tibial Tray — Class II medical device recall Z-2518-2019
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-2518-2019 |
|---|---|
| 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 | 384 units |
| Lot numbers | 011510, 018270, 023420, 029310, 061480, 073030, 076780, 089950, 093450, 093460, 103080, 116110, 116110R, 126090, 126100, 131270, 159350, 163080, 163090, 181490, 183670, 191210, 219890, 223220, 247440, 283080, 283100, 293200, 293210, 318630, 321690, 321710, 321750, 321770, 331670, 358830, 358840, 358850, 358860, 374570 and 70 more |
| Model numbers | 195759 |
Product
XP-XP Tibial Tray - Interlok 83 mm Item # 195759
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-2518-2019. 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.