Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
NORepinephrine Bitartrate Recalled by Pharmedium Services, LLC Due to Subpotent Drug; confirmed results by FDA analysis after...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Pharmedium Services, LLC directly.
Affected Products
NORepinephrine Bitartrate, 8 mg (32 mcg/mL) added to 250 mL 0.9% Sodium Chloride Injection USP, in 250 mL Viaflex Bag Black, Rx only, PharMEDium Services, LLC, Sugar Land, TX NDC 61553-127-61
Why Was This Recalled?
Subpotent Drug; confirmed results by FDA analysis after customer complaints of discoloration
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Pharmedium Services, LLC
Pharmedium Services, LLC has 246 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report