# FDA recall Z-1901-2024

> **Smith & Nephew Inc** · Class II · device recall initiated 2024-04-24.

## Product

smith&nephew OXINIUM Femoral Head 12/14 Taper, REF 71343204, 32 MM OD +4, Sterile; and smith&nephew, 12/14 Taper, REF 71343604, 36 MM M / +4

## Reason for recall

Packaging contained the incorrect size of femoral head from what was displayed on the label.

## Distribution

International distribution to the countries of Australia, Germany, Japan, Portugal, and United Kingdom.

## Key facts

- **Recall number:** Z-1901-2024
- **Recalling firm:** Smith & Nephew Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-04-24
- **Report date:** 2024-06-05

- **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-1901-2024

## Citation

> AI Analytics. FDA recall Z-1901-2024. Retrieved 2026-07-15 from https://api.ai-analytics.org/recall/Z-1901-2024. Source: US FDA. Licensed CC0.

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