SCA Pharmaceuticals recalls hydro morphine injections with lack of sterility assurance. Affected lots expire by December 2023. Consumers should contact the manufacturer for details.
Lack of Assurance of Sterility
SCA Pharmaceuticals is recalling hydro morphine injections due to a lack of sterility assurance. This could lead to infections if the product is used. The recall affects specific lots with expiration dates through December 2023.
The product lacks sterility assurance, meaning it may contain harmful bacteria or contaminants. If injected, this could cause serious infections or other health issues. The risk is particularly concerning for medical use where sterility is critical.
Prescription users of hydro morphine injections with specific lot numbers and expiration dates through December 2023. Healthcare professionals and patients using the recalled product are at risk of infection.
Check the lot number on the syringe label. The affected lots include 1223048801 (exp 12/04/23), 1223049225 (exp 12/21/23), 1223049264 (exp 12/25/23), 1223049291 (exp 12/26/23), and 1223049726 (exp 01/11/24).
Look for the lot number on the syringe label to determine if it is affected.
Hydro morphine HCl 10 mg/50 mL in 0.9% Sodium Chloride Injection (Concentration = 0.2 mg/ml) 50 mL fill Syringe, Rx only.
Lack of assurance of sterility, which could lead to infections if the product is used.
Check the lot number on the syringe label. Affected lots include 1223048801 (exp 12/04/23), 1223049225 (exp 12/21/23), 1223049264 (exp 12/25/23), 1223049291 (exp 12/26/23), and 1223049726 (exp 01/11/24).
We’ve drafted a message you can send SCA Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0407-2024 — SCA Pharmaceuticals SCA Pharmaceuticals Hello, I own a SCA Pharmaceuticals that is covered by recall D-0407-2024 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.
