FDA Device recall Z-2513-2019
XP-CR Tibial Tray - Interlok 87 mm Item # 195278
- FDA Device
- Class II
- terminated
- Published 2019-09-18
On 2019-09-18 the FDA classified a Class II recall of XP-CR Tibial Tray - Interlok 87 mm Item # 195278 by Zimmer Biomet, citing the locking bar not fully engaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2513-2019 |
| 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
XP-CR Tibial Tray - Interlok 87 mm Item # 195278
Reason
The locking bar not fully engaging
Identifiers
| code_info | Lot Number 966230 262470 587200 274370 274360 274380 274420 715690 274420R 715690R 393650 279080 394490 821380 903430 943440 422480 512580 |
|---|
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-2513-2019%22
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