# FDA recall Z-1470-2020

> **Integra LifeSciences Corp.** · Class III · device recall initiated 2020-02-07.

## Product

NeuraGen Nerve Guide, 7mm diameter, 2cm length; Part number PNG72 - Product Usage: NeuraGen nerve guide is indicated for the repair of peripheral nerve discontinuities where gap closure can be achieved by flexion of the extremity.

## Reason for recall

Nonconforming product which was dispositioned for rejection was mistakenly released for commercial use.

## Distribution

Worldwide distribution - US Nationwide distribution in the states of AZ, CA, CO, IN, LA, MI, MN, MO, NC, NM, NY, PA, SC, and TX and countries of Italy, France, Germany, and Finland.

## Key facts

- **Recall number:** Z-1470-2020
- **Recalling firm:** Integra LifeSciences Corp.
- **Classification:** Class III
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-02-07
- **Report date:** 2020-03-18
- **Termination date:** 2020-06-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Princeton, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1470-2020

## Citation

> AI Analytics. FDA recall Z-1470-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1470-2020. Source: US FDA. Licensed CC0.

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