SCA Pharmaceuticals recalls Oxytocin 30 units in 0.9% Sodium Chloride 500mL for subpotent drug results. This medication may not work as intended when used for medical purposes.
Subpotent Drug: Out of specification results for low potency was obtained.
SCA Pharmaceuticals is recalling Oxytocin 30 units added to 0.9% Sodium Chloride 500 mL because it has subpotent results, meaning it may not work as intended when used for medical purposes. This affects patients who require this medication for specific medical treatments.
The medication has been found to have lower potency than specified, meaning it may not provide the intended therapeutic effect. This could lead to inadequate treatment outcomes for patients requiring this medication for medical procedures.
Patients prescribed this medication by a healthcare provider. Those using it for medical treatments are most at risk of receiving an ineffective dose.
Check for the product name 'Oxytocin 30 units added to 0.9% Sodium Chloride 500 mL', manufactured by SCA Pharmaceuticals, with NDC# 70004-085-44. Lot numbers range from 1222043028 to 1223044868 as listed in the recall notice.
Verify the product name, manufacturer, and lot numbers listed in the recall notice to confirm if your medication is affected.
The recall indicates the medication may not work as intended due to subpotent results, so it should not be used until the recall is addressed.
Check for the product name 'Oxytocin 30 units added to 0.9% Sodium Chloride 500 mL' with manufacturer SCA Pharmaceuticals and NDC# 70004-085-44. Lot numbers range from 1222043028 to 1223044868.
The recall does not specify a remedy, so contact your healthcare provider for guidance on whether to continue using the medication or seek alternatives.
We’ve drafted a message you can send SCA Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0555-2023 — SCA Pharmaceuticals SCA Pharmaceuticals Hello, I own a SCA Pharmaceuticals that is covered by recall D-0555-2023 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.
