Short Fill: The product is being recalled due to a potential underfill of the affected vials.
Short Fill: The product is being recalled due to a potential underfill of the affected vials.
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send Bracco Diagnostics Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-1663-2012 — Bracco Diagnostics Inc. Bracco Diagnostics Inc recalls Bracco Diagnostics multihance (gadobenate di Hello, I own a Bracco Diagnostics Inc recalls Bracco Diagnostics multihance (gadobenate dimeglumine) injection, 529 mg/mL, 20ml, Rx only, Manufactured for: Bracco that is covered by recall D-1663-2012 from Bracco Diagnostics Inc.. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
