# FDA recall Z-2621-2023

> **Smith & Nephew Inc** · Class II · device recall initiated 2023-08-31.

## Product

smith&nephew LEGION OXINUM POSTERIOR STABILIZED NONPOROUS FERMOAL COMPONENT, SIZE 5N, LEFT, NARROW, REF 71421265; knee joint

## Reason for recall

The firm conducting a recall due to a complaint received indicating that a package contained a LEGION NARROW PS OXIN SZ 4N LT implant instead of a LEGION NARROW PSvOXIN SZ 5N LT as described on the product label.

## Distribution

OH, CT, TX, NC, CA, NE, NV

## Key facts

- **Recall number:** Z-2621-2023
- **Recalling firm:** Smith & Nephew Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-08-31
- **Report date:** 2023-09-27

- **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-2621-2023

## Citation

> AI Analytics. FDA recall Z-2621-2023. Retrieved 2026-08-21 from https://api.ai-analytics.org/recall/Z-2621-2023. Source: US FDA. Licensed CC0.

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