SCA Pharmaceuticals recalls phenylephrine injections with potential lack of sterility. Affected lots expire by 2024; consumers should contact the manufacturer for details.
Lack of Assurance of Sterility
SCA Pharmaceuticals is recalling phenylephrine injections that may not be sterile. This could lead to infections if used improperly. The product is prescription-only and must be checked for specific lot numbers.
The injections may not be sterile, which can cause infections if the product is used. This is a serious risk for medical procedures where contamination could lead to health issues.
Prescription patients who received phenylephrine injections with the listed lot numbers. Those using the product for medical procedures are at higher risk due to potential contamination.
Check the product label for the lot numbers listed: 1223045536 through 1223049980. The expiration dates range from December 2023 to June 2024. The product is prescription-only and sold under NDC 70004-0810-12.
Look for the lot numbers listed: 1223045536 through 1223049980 on the injection vial.
Reach out to SCA Pharmaceuticals at 755 Rainbow Rd., Windsor, CT 06095 for further assistance.
The recall indicates a lack of sterility assurance, which could lead to infections. The product is not safe for use without checking the lot numbers.
Check the product label for lot numbers between 1223045536 and 1223049980. The expiration dates range from December 2023 to June 2024.
Contact SCA Pharmaceuticals at 755 Rainbow Rd., Windsor, CT 06095 to 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-0414-2024 — SCA Pharmaceuticals SCA Pharmaceuticals Hello, I own a SCA Pharmaceuticals that is covered by recall D-0414-2024 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.
