# FDA recall Z-0406-2018

> **Smith & Nephew, Inc.** · Class II · device recall initiated 2017-10-23.

## Product

Radial Osteotome Blade, REF 71369314.    Used for cutting or preparing bone.

## Reason for recall

The expiration date provided on the label is incorrect.

## Distribution

Worldwide Distribution -- US, to the states of TN and NJ; and, Australia.

## Key facts

- **Recall number:** Z-0406-2018
- **Recalling firm:** Smith & Nephew, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-10-23
- **Report date:** 2018-01-31
- **Termination date:** 2018-08-24

- **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-0406-2018

## Citation

> AI Analytics. FDA recall Z-0406-2018. Retrieved 2026-07-12 from https://api.ai-analytics.org/recall/Z-0406-2018. Source: US FDA. Licensed CC0.

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