SCA Pharmaceuticals recalls phenylephrine HCl 40mg injection (NDC 70004-0825-40) due to lack of sterility assurance. This product may cause infections if used.
Lack of Assurance of Sterility
SCA Pharmaceuticals is recalling phenylephrine HCl 40 mg injection (250 mL) because it lacks sterility assurance. Using this product could lead to infections, especially in medical settings where sterile injections are critical.
The product lacks sterility assurance, meaning it may contain contaminants that could cause infections when injected. This is a risk in medical settings where sterile injections are critical.
Patients prescribed this injection by a healthcare provider. Those using it for medical purposes are most at risk.
Check for the product name 'Phenylephrine HCl 40 mg in 0.9% Sodium Chloride Injection', 250 mL bag, with NDC 70004-0825-40. It was sold by SCA Pharmaceuticals with lot number 1223050005, expiring January 13, 2024.
Verify the product name, NDC 70004-0825-40, and lot number 1223050005 on the label.
No, this product lacks sterility assurance and may cause infections if used.
Look for the product name 'Phenylephrine HCl 40 mg in 0.9% Sodium Chloride Injection', 250 mL bag, with NDC 70004-0825-40 and lot number 1223050005.
Check the product details and contact your healthcare provider for guidance.
We’ve drafted a message you can send SCA Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0419-2024 — SCA Pharmaceuticals SCA Pharmaceuticals Hello, I own a SCA Pharmaceuticals that is covered by recall D-0419-2024 from SCA Pharmaceuticals. 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.
