Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

The UNI-CP System Recalled by Integra LifeSciences Corp. Due to The firm received one complaint from one non-US...

Date: January 25, 2017
Company: Integra LifeSciences Corp.
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Integra LifeSciences Corp. directly.

Affected Products

The UNI-CP System; Model Number: 330230SND.

Quantity: 39 units

Why Was This Recalled?

The firm received one complaint from one non-US sales representative (France) that the label on the UNI-CP plate was incorrect.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Integra LifeSciences Corp.

Integra LifeSciences Corp. has 216 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report