Lack of Assurance of Sterility; Product recalled due to displacement of the aluminum crimp cap during product usage.
Lack of Assurance of Sterility; Product recalled due to displacement of the aluminum crimp cap during product usage.
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-1665-2012 — Bracco Diagnostics Inc. Bracco Diagnostics Inc recalls Multihance Multipack (gadobenate dimeglumine Hello, I own a Bracco Diagnostics Inc recalls Multihance Multipack (gadobenate dimeglumine) injection, 529 mg/mL, Pharmacy Bulk Package - Not for Direct Infusion, that is covered by recall D-1665-2012 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.
