Lack of Sterility Assurance: The product has the potential to leak at the administrative port.
Lack of Sterility Assurance: The product has the potential to leak at the administrative port.
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 Hospira Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-0490-2015 — Hospira Inc. Hospira Inc. recalls 0.9% Sodium Chloride Injection, USP, 100 mL ADD-Vantage Unit, Rx Hello, I own a Hospira Inc. recalls 0.9% Sodium Chloride Injection, USP, 100 mL ADD-Vantage Unit, Rx only, Manufactured by Hospira Inc., Lake Forest, IL, that is covered by recall D-0490-2015 from Hospira 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.
