Class III โ€” Low Risk

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

VoLumen Barium Sulfate Suspension (0.1 % w/v Recalled by Bracco Diagnostics Inc Due to Failed Stability Testing: This product is below specification...

Date: December 16, 2013
Company: Bracco Diagnostics Inc
Status: Terminated
Source: FDA (Drug)

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 Bracco Diagnostics Inc directly.

Affected Products

VoLumen Barium Sulfate Suspension (0.1 % w/v, 0.1 ww/w), 450 mL bottle, Rx Only. Manufactured by E-Z-EM Canada Inc. a subsidiary or E-Z-EM, Inc. Lake Success, NY 11042. NDC 32909-945-03.

Quantity: 54,648 bottles

Why Was This Recalled?

Failed Stability Testing: This product is below specification for preservative content.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Bracco Diagnostics Inc

Bracco Diagnostics Inc has 6 total recalls tracked by RecallDetector.

Related Recalls

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