Zimmer Biomet, Inc.: Medical Device Recall in 2019 - (Recall #: Z-2505-2019)

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 65mm Item # 195270

Product Classification:

Class II

Date Initiated: August 15, 2019

Date Posted: September 18, 2019

Recall Number: Z-2505-2019

Event ID: 83594

Reason for Recall:

The locking bar not fully engaging

Status: Terminated

Product Quantity: 375 units

Code Information:

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

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