# FDA recall Z-0910-2022

> **Nextremity Solutions** · Class II · device recall initiated 2022-02-10.

## Product

Nextra Hammertoe Correction System 4.5 Middle 3.2 Proximal Kit   SKU: NX-4532K    Orthopedic surgical instrument

## Reason for recall

Proximal end of the driver is oversized in varying degrees, making it difficult to fully connect with and remove from the proximal Nextra implant, causing delay in surgery

## Distribution

Distribution US Nationwide, Japan, and the Netherlands

## Key facts

- **Recall number:** Z-0910-2022
- **Recalling firm:** Nextremity Solutions
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-02-10
- **Report date:** 2022-04-20
- **Termination date:** 2024-10-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Warsaw, IN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0910-2022

## Citation

> AI Analytics. FDA recall Z-0910-2022. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-0910-2022. Source: US FDA. Licensed CC0.

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