Zimmer Biomet, Inc.: Medical Device Recall in 2019 - (Recall #: Z-2506-2019)

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 67mm Item # 195271

Product Classification:

Class II

Date Initiated: August 15, 2019

Date Posted: September 18, 2019

Recall Number: Z-2506-2019

Event ID: 83594

Reason for Recall:

The locking bar not fully engaging

Status: Terminated

Product Quantity: 567 units

Code Information:

Lot Number 486100 262400 291180 584260 663550 562250 666830 660450 841520 917700 966720 966720R 075450 075460 075500 663530 995960 322020 043860 090190 206820 075440 745670 352820 383680 075470 745650 513340 159230 258060 429230 161960 161950 161930 161910 161920 162010 161860 274480 161870 161900 274460 996070 274490 274510 721690 322000 456750 456750R 274470 374780 951150 075510 469490 721670 309710 274500 309680 309690 075490 309700 585540 883560 221140 374030 920540 279010 450330 672510 575980 821280 943360 599120 600770 712550 717160 017970 076400 076410 220040 175290 175290R 289160 676270 676300 228610 351290 395400 395420 445370 395400R

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