Lack of Assurance of Sterility: There is the potential for the solution to leak from the seal of the fill tube to the bag.
Lack of Assurance of Sterility: There is the potential for the solution to leak from the seal of the fill tube to the bag.
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-184-2013 — Hospira Inc. Hospira Inc. recalls HEXTEND 6% Hetastarch in Lactated Electrolyte Injection, 500 mL, R Hello, I own a Hospira Inc. recalls HEXTEND 6% Hetastarch in Lactated Electrolyte Injection, 500 mL, Rx only , MANUFACTURED AND DISTRIBUTED BY HOSPIRA, that is covered by recall D-184-2013 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.
