Labeling: Label Error on Declared Strength
Labeling: Label Error on Declared Strength
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 Jubilant Draximage Inc to request your refund or repair — edit it as you like.
Subject: Recall D-0812-2016 — Jubilant Draximage Inc Jubilant Draximage Inc recalls SODIUM IODIDE I 131 CAPSULE, USP DIAGNOSTIC O Hello, I own a Jubilant Draximage Inc recalls SODIUM IODIDE I 131 CAPSULE, USP DIAGNOSTIC ORAL , Rx only, Manufactured by Jubilant DraxImage, Inc., Kirkland, QC, that is covered by recall D-0812-2016 from Jubilant Draximage 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.
