# FDA recall Z-0730-2019

> **Smith & Nephew, Inc.** · Class II · device recall initiated 2019-01-07.

## Product

SL PLUS MIA DOUBLE OFFSET ADAPTER RIGHT 60/25MM, S&N 75004613

## Reason for recall

The pin that holds the spring mechanism is not properly mounted. The pin could potentially disassemble.

## Distribution

NY, TN, Germany, Italy, Great Britain, Singapore

## Key facts

- **Recall number:** Z-0730-2019
- **Recalling firm:** Smith & Nephew, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-01-07
- **Report date:** 2019-01-23
- **Termination date:** 2020-09-17

- **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-0730-2019

## Citation

> AI Analytics. FDA recall Z-0730-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0730-2019. Source: US FDA. Licensed CC0.

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