# FDA recall Z-1099-2022

> **Smith & Nephew Inc** · Class II · device recall initiated 2022-04-19.

## Product

LEGION NARROW PS OXIN SZ 6N RT and JRNY II BCS FEMORAL OXIN LT SZ 5

## Reason for recall

It was reported that a JOURNEY II BCS Femoral OXIN LT SZ5 was in a box labelled as a LEGION NARROW PS OXIN SZ 6N RT.

## Distribution

Worldwide distribution - US Nationwide distribution in the states of CT, NC, CO, SC, VA, FL, IL, CA and the country of Japan.

## Key facts

- **Recall number:** Z-1099-2022
- **Recalling firm:** Smith & Nephew Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-04-19
- **Report date:** 2022-05-25
- **Termination date:** 2024-08-16

- **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-1099-2022

## Citation

> AI Analytics. FDA recall Z-1099-2022. Retrieved 2026-06-12 from https://api.ai-analytics.org/recall/Z-1099-2022. Source: US FDA. Licensed CC0.

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