Zimmer Biomet, Inc.: Medical Device Recall in 2019 - (Recall #: Z-2525-2019)

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-XP Tibial Tray - Interlok 65 mm Item # 195752

Product Classification:

Class II

Date Initiated: August 15, 2019

Date Posted: September 18, 2019

Recall Number: Z-2525-2019

Event ID: 83594

Reason for Recall:

The locking bar not fully engaging

Status: Terminated

Product Quantity: 857 units

Code Information:

Lot Number 590800 309530 579280 309460 590810 590820 309510 650390 562160 613330 758190 571150 589750 972670 029010 065310 029010R 206950 043980 065640 174940 043980R 174930 206930 257980 336590 206940 257990 028990 029000 783130 783160 801980 801980R 783100 885030 916820 864690 958350 958350R 783120 783150 855240 958340 840660 801970 023350 783080 036230 975570 984720 984740 011420 103000 159280 093370 061330 115950 131180 181380 297160 309500 511440 599700 467150 634140 664150 684850 664150R 587250 309480 705540 328040 715740 716040 241420 261140 882060 920560 029220 072830 906660 985890 396310 125970 162900 162920 221350 076130 247260 318440 374340 336670 374370 293080 441880 478800 478820 509650 509620 076090 543210 543230 576090 559000 559000R 576100 593570 450410 522600 639610 670520 708400 741480 741470 758490 780170 833160 183380 808180 850890 917600 873480 873490 963440 999290 999290R 943500 560300 570190 570200 018080 076650 137480 111640 191100 579300 219730 289200 261920

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