# FDA recall Z-0740-2022

> **Nextremity Solutions** · Class II · device recall initiated 2022-01-13.

## Product

Nextra Cannulated Hammertoe Standard Instrument Kit-indicated for small bone reconstruction limited to inter-digital repair and fusion of the lesser toe  SKU: CH-STD-KT

## Reason for recall

During insertion of the middle phalanx implant into bone, the driver may deform the implant locking mechanism and result in inadequate mating force between the middle and proximal phalanx implants, resulting in surgical delay, in-situ removal of the implant, use of alternative surgical approach, disassembly of the implants post-operatively, and revision

## Distribution

US Nationwide distribution in the states of AZ, IL, GA, LA, MD, NY, PA, TX, WA.

## Key facts

- **Recall number:** Z-0740-2022
- **Recalling firm:** Nextremity Solutions
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-01-13
- **Report date:** 2022-03-16
- **Termination date:** 2024-05-24

- **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-0740-2022

## Citation

> AI Analytics. FDA recall Z-0740-2022. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0740-2022. Source: US FDA. Licensed CC0.

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