RecallRadar

FDA Drug recall D-1663-2012

Bracco Diagnostics multihance (gadobenate dimeglumine) injection, 529 mg/mL, 20ml, Rx only, Manufactured for: Bracco Diagnostics Inc., Prin…

On 2012-09-05 the FDA classified a Class III recall of Bracco Diagnostics multihance (gadobenate dimeglumine) injection, 529 mg/mL, 20ml, Rx only, Manufactured for: Bracco Diagnostics Inc., Prin… by Bracco Diagnostics, citing short Fill: The product is being recalled due to a potential underfill of the affected vials.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1663-2012
ClassificationClass III
Statusterminated
Initiated2012-04-16
Published2012-09-05
Last updated2026-09-13 11:51 UTC
CompanyBracco Diagnostics
DistributionUS

Product

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

Reason

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

Identifiers

ndc0270-5164-12
ndc0270-5164-13
ndc0270-5164-14
ndc0270-5164-15
code_infoLot S1P272A Expiry Date: December 2014

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1663-2012%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.