# FDA recall Z-1324-2021

> **Nuvasive Specialized Orthopedics Inc** · Class II · device recall initiated 2021-02-12.

## Product

Precice Bone Transport  - Product Usage:  intended for limb lengthening, open and closed fracture fixation, pseudoarthrosis, mal-unions, non-unions, or bone transport of long bones.

## Reason for recall

Due to complaints of adverse events potentially related to biological safety.  The complaints included report of pain and bony abnormalities at the interface between the telescoping nail segments.

## Distribution

Worldwide distribution - U.S. Nationwide distribution and the countries of Argentina, Austria, Belgium, Canada, Chile, Colombia, Cyprus, Denmark, Finland, France, Germany, Greece, Hong Kong, Israel, Italy, Luxemburg, Netherlands, Portugal, Saudi Arabia, Slovakia, Slovenia, South Africa, Spain, Sweden, Switzerland, Turkey and UAE.    Consignee List provided only includes email addresses.  Complete contact information is pending.

## Key facts

- **Recall number:** Z-1324-2021
- **Recalling firm:** Nuvasive Specialized Orthopedics Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2021-02-12
- **Report date:** 2021-04-07

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Aliso Viejo, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1324-2021

## Citation

> AI Analytics. FDA recall Z-1324-2021. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1324-2021. Source: US FDA. Licensed CC0.

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