SCA Pharmaceuticals recalls hydro morphine injection (NDC 70004-0303-21) due to lack of sterility assurance. Products may cause infection if used improperly. Contact for return instructions.
Lack of Assurance of Sterility
SCA Pharmaceuticals is recalling hydro morphine injections that may not be sterile, posing an infection risk. This affects patients using the medication as prescribed by a doctor.
The injection may not be sterile, which could lead to infections if used improperly. This is a risk during medical procedures where the product is administered directly into the body.
Patients prescribed hydro morphine injections by a doctor. Those using the product without medical supervision are not affected.
Look for the product name 'Hydro morphine HCl 30 mg/30 mL in 0.9% Sodium Chloride Injection' with NDC 70004-0303-21. Products were sold with specific lot numbers and expiration dates listed in the recall notice.
Verify the product's NDC number is 70004-0303-21 and check the lot number and expiration date on the label.
The recall states there is a lack of sterility assurance, so it is not safe to use without the remedy.
The recall record does not specify replacement options or instructions for returns.
The recall record does not provide specific action steps for affected users.
We’ve drafted a message you can send SCA Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0410-2024 — SCA Pharmaceuticals SCA Pharmaceuticals Hello, I own a SCA Pharmaceuticals that is covered by recall D-0410-2024 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.
