# FDA recall Z-1418-2022

> **Smith & Nephew, Inc.** · Class II · device recall initiated 2022-06-27.

## Product

(1) Genesis II Non-Porous Tibial Baseplate Size 5 Right, Product #71420186.  (2) Genesis II Non-Porous Tibial Baseplate Size 4 Left, Product #71420166.

## Reason for recall

The product was mispackaged (swapped).  The devices within the inner tray matches the inner tray but does not match the outer box label and the chart sticks.

## Distribution

US Nationwide distribution in the states of AZ, CA, GA, KS, LA, MN, MI, MO, MS, NC, NJ, NY, OR, SC, TN, VA, WA, and WI.

## Key facts

- **Recall number:** Z-1418-2022
- **Recalling firm:** Smith & Nephew, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-06-27
- **Report date:** 2022-07-27
- **Termination date:** 2026-03-25

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Memphis, TN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1418-2022

## Citation

> AI Analytics. FDA recall Z-1418-2022. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1418-2022. Source: US FDA. Licensed CC0.

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