# FDA recall Z-2533-2019

> **Zimmer Biomet, Inc.** · Class II · device recall initiated 2019-08-15.

## Product

Vanguard XP Tibial Tray 73 mm  Item # 195250

## Reason for recall

The locking bar not fully engaging

## Distribution

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

## Key facts

- **Recall number:** Z-2533-2019
- **Recalling firm:** Zimmer Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-08-15
- **Report date:** 2019-09-18
- **Termination date:** 2021-04-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Warsaw, IN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2533-2019

## Citation

> AI Analytics. FDA recall Z-2533-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2533-2019. Source: US FDA. Licensed CC0.

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