Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
NORepinephrine Bitartrate 8 mg added to 250 mL 5% Dextrose Recalled by Pharmedium Services, LLC Due to Subpotent Drug
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 added to 250 mL 5% Dextrose Injection USP (32 mcg per mL) Total Volume 258.00 mL Viaflex Bag, High Alert, Rx Only, PharMEDium Services LLC., 12620 W Airport Blvd #130 Sugar Land, TX 77478.
Quantity: 5820 bags
Why Was This Recalled?
Subpotent Drug
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