Lack of Assurance of Sterility: Either a loose crimp or no crimp was applied to the fliptop vials.
Lack of Assurance of Sterility: Either a loose crimp or no crimp was applied to the fliptop 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 Hospira Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-926-2013 — Hospira Inc. Hospira, Inc. recalls Ketorolac Tromethamine Inj., USP, 30 mg vial, Rx only, Hospira, I Hello, I own a Hospira, Inc. recalls Ketorolac Tromethamine Inj., USP, 30 mg vial, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-3795-01 that is covered by recall D-926-2013 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.
