FDA Device recall Z-2505-2019
XP-CR Tibial Tray - Interlok 65mm Item # 195270
- 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 65mm Item # 195270 by Zimmer Biomet, citing the locking bar not fully engaging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2505-2019 |
| 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 65mm Item # 195270
Reason
The locking bar not fully engaging
Identifiers
| code_info | Lot Number 666880 660440 579080 579170 993790 262390 228590 584250 289150 579150 663480 996060 663480R 04…Lot Number 666880 660440 579080 579170 993790 262390 228590 584250 289150 579150 663480 996060 663480R 043850 090170 917690 159220 321940 352810 374770 600760 663500 841510 076020 352800 383660 429220 966710 321970 456740 456740R 995950 258050 274610 274600 403820 206810 041210 899720 899760 585520 585520R 041280 503430 437500 503490 503420 247240 247240R 374010 712540 672470 279000 575960 017940 450320 599100 717150 599100R 943350 821270 111560 220030 175280 199800 199810 175280R 395360 395370 395390 445360 395390R |
|---|
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-2505-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.