# FDA recall Z-2177-2018

> **Zimmer Biomet, Inc.** · Class II · device recall initiated 2018-05-18.

## Product

Biomet Modular Primary Tibial Tray Implants; Modular Interlok Primary Tray (size 75 mm); Item No. 141215; UDI: (01) 00880304005310 (17) 280306 (10) 385340    Product is used in Total Knee Arthroplasty

## Reason for recall

One lot of 75mm tibial tray is potentially etched and labeled as a 79 mm tibial tray. This may lead to delay in surgery, or immediate revision surgery to remove an incorrectly sized tibial component after it has been cemented.

## Distribution

US Distribution to the states of : FL, GA, IN, MA, NM, UT, and WI. Foreign distribution to Canada and Mexico

## Key facts

- **Recall number:** Z-2177-2018
- **Recalling firm:** Zimmer Biomet, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-05-18
- **Report date:** 2018-06-20
- **Termination date:** 2020-03-31

- **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-2177-2018

## Citation

> AI Analytics. FDA recall Z-2177-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2177-2018. Source: US FDA. Licensed CC0.

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