Labeling: Label mix-up - ephedrine syringes mislabeled as phenylephrine.
Labeling: Label mix-up - ephedrine syringes mislabeled as phenylephrine.
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 Hikma Injectables USA Inc to request your refund or repair — edit it as you like.
Subject: Recall D-0508-2024 — Hikma Injectables USA Inc Hikma Injectables USA Inc recalls Phenylephrine in 0.9% Sodium Chloride I Hello, I own a Hikma Injectables USA Inc recalls Phenylephrine in 0.9% Sodium Chloride Injection Preservative Free, 100mcg/mL, 5mL syringe, Rx only, Hikma Injectables that is covered by recall D-0508-2024 from Hikma Injectables USA 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.
