Class III — Low Risk

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

Heliomolar Refill 20x0.25g 110T Recalled by Ivoclar Vivadent, Inc. Due to Complaints were filed claiming the material consistency was...

Date: August 3, 2017
Company: Ivoclar Vivadent, Inc.
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 Ivoclar Vivadent, Inc. directly.

Affected Products

Heliomolar Refill 20x0.25g 110T, Product code 550559AN, Catalog number 550559

Quantity: 2 units

Why Was This Recalled?

Complaints were filed claiming the material consistency was too soft and too sticky in comparison to its usual consistency, causing unexpected handling for the user during packing and contouring.

Where Was This Sold?

US and Canada

About Ivoclar Vivadent, Inc.

Ivoclar Vivadent, Inc. has 34 total recalls tracked by RecallDetector.

Related Recalls

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