Zimmer Biomet, Inc.: Medical Device Recall in 2019 - (Recall #: Z-2509-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

XP-CR Tibial Tray - Interlok 73mm Item # 195274

Product Classification:

Class II

Date Initiated: August 15, 2019

Date Posted: September 18, 2019

Recall Number: Z-2509-2019

Event ID: 83594

Reason for Recall:

The locking bar not fully engaging

Status: Terminated

Product Quantity: 327 units

Code Information:

Lot Number 553880 590760 663690 553880R 590750 663670 262430 513080 663720 513080R 472990 938180 578980 090230 159280 676320 258090 043920 066220 206850 322110 352860 841550 917740 966760 283230 374810 283240 996010 352850 352850R 429270 851300 383710 041300 585600 076010 469520 578970 599150 600800 600800R 279040 450360 672600 374090 943410 712580 121150 018040 821330 121140 199740 218670 717190 308100 308110 502840 513070 571040 502840R 513070R 571040R

Distribution Pattern:

State NY IN OH MI GA SC FL MO WI MN ND SD NE NJ PA MD IL IA CA VA NC DC WV AR AL MS AL MI WA OR ID LA FL KS TN MA KY OK TX TX CT AZ NV NM MT WY CO UT DC WY Country: KOREA CHINA CANADA AUSTRALIA JAPAN EMEA SWEDEN ITALY

Voluntary or Mandated:

Voluntary: Firm initiated