SCA Pharmaceuticals recalls specific lots of phenylephrine HCl injection (5000 mcg/50mL) due to lack of sterility assurance. This could lead to infections if used improperly. Consumers should check lot numbers and contact the manufacturer for details.
Lack of Assurance of Sterility
SCA Pharmaceuticals is recalling certain lots of phenylephrine HCl injection (5000 mcg/50 mL) because they lack sterility assurance. This means the product could cause infections if used, especially in medical settings where sterility is critical.
The injection product lacks proper sterility assurance, meaning it could contain harmful bacteria or contaminants. If used in medical procedures, this could lead to infections, particularly in sensitive areas like injections.
Patients prescribed this medication by a healthcare provider. Those using the product for medical purposes are most at risk due to potential infection from non-sterile injections.
Check the lot numbers listed in the recall: 1223045282 through 1223050181. The expiration dates range from November 2023 to June 2024. The product is a prescription-only phenylephrine injection with a 50 mL syringe.
Look for the lot number on the product label, which is listed in the recall (e.g., 1223045282 to 1223050181).
Reach out to SCA Pharmaceuticals at 755 Rainbow Rd., Windsor, CT 06095 for further assistance or to confirm if your product is affected.
The product has been recalled due to lack of sterility assurance, which could lead to infections. It is not safe to use without confirming it's not part of the recalled lots.
Check the lot number on the product label; the affected lots range from 1223045282 to 1223050181 as listed in the recall notice.
Contact SCA Pharmaceuticals at 755 Rainbow Rd., Windsor, CT 06095 to confirm if your product is affected and get further instructions.
We’ve drafted a message you can send SCA Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0417-2024 — SCA Pharmaceuticals SCA Pharmaceuticals Hello, I own a SCA Pharmaceuticals that is covered by recall D-0417-2024 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.
