Class III โ€” Low Risk

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

Bracco Diagnostics multihance (gadobenate dimeglumine) injection Recalled by Bracco Diagnostics Inc Due to Short Fill: The product is being recalled due...

Date: April 16, 2012
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

Bracco Diagnostics multihance (gadobenate dimeglumine) injection, 529 mg/mL, 20ml, Rx only, Manufactured for: Bracco Diagnostics Inc., Princeton, NJ 08543 USA, NDC 0270-5164-15

Quantity: 47,750 vials

Why Was This Recalled?

Short Fill: The product is being recalled due to a potential underfill of the affected vials.

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