Data Foundry

Medical device recalls 2019

XP-XP Tibial Tray — Class II medical device recall Z-2526-2019

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 numberZ-2526-2019
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmZimmer Biomet, Inc., Warsaw, IN, United States
Recall initiated2019-08-15
Classified2019-09-12
Reported by FDA2019-09-18
Terminated2021-04-16
DistributedAL, 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 USAU, CA, CN, IT, JP, KR, SE
Quantity480 units
Lot numbers011410, 018060, 023340, 028960, 028970, 028980, 028980R, 029210, 043970, 043970R, 061310, 064960, 065200, 065200R, 072790, 076640, 101860, 101880, 102990, 111620, 125870, 162880, 183370, 191080, 223050, 247250, 257960, 257970, 261130, 261910, 282690, 282710, 282710R, 318430, 321620, 321620R, 321640, 321640R, 336080, 336660 and 69 more
Model numbers195751

Product

XP-XP Tibial Tray - Interlok 63 mm Item # 195751

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-2526-2019. 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.