Zimmer Biomet, Inc.: Medical Device Recall in 2019 - (Recall #: Z-2533-2019)

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:

Vanguard XP Tibial Tray 73 mm Item # 195250

Product Classification:

Class II

Date Initiated: August 15, 2019

Date Posted: September 18, 2019

Recall Number: Z-2533-2019

Event ID: 83594

Reason for Recall:

The locking bar not fully engaging

Status: Terminated

Product Quantity: 84 units

Code Information:

Lot Number 590540 590530 590520 663190 590550 663200 907710 117740 332690 833210 752580 373050 373060 515050 752120 515070 752100 752110 754490 764390 861210 837790 936210 764400 846520 928890 907690 936220 936230 954050 928880 936200 954030 907700 063000 062990 570980 584230

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