Zimmer Biomet, Inc.: Medical Device Recall in 2019 - (Recall #: Z-2534-2019)

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 75 mm Item # 195251

Product Classification:

Class II

Date Initiated: August 15, 2019

Date Posted: September 18, 2019

Recall Number: Z-2534-2019

Event ID: 83594

Reason for Recall:

The locking bar not fully engaging

Status: Terminated

Product Quantity: 110 units

Code Information:

Lot Number 833220 919250 919260 936260 764410 764420 837800 936240 846540 861190 928760 936250 954020 846530 928770 953990 928800 954000 928790 590580 571000 663280 590570 663250 663260 663270 590590 663240 663300 590560 332710 515110 373070 373080 515090 752140 752130 332740 754500

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