Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
HYDROmorphone HCl 25 mg/25 mL in 0.9% Sodium Chloride Injection Recalled by SCA Pharmaceuticals, LLC Due to Lack of Assurance of Sterility
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 SCA Pharmaceuticals, LLC directly.
Affected Products
HYDROmorphone HCl 25 mg/25 mL in 0.9% Sodium Chloride Injection, (Concentration = 1mg/mL), 25 mL fill 30 mL Syringe, Rx only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0303-17, Bar Code 7004030317
Quantity: 399 syringes
Why Was This Recalled?
Lack of Assurance of Sterility
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About SCA Pharmaceuticals, LLC
SCA Pharmaceuticals, LLC has 56 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report