Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Ketamine 50 mg/5 mL in 0.9% Sodium Chloride Injection for 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
Ketamine 50 mg/5 mL in 0.9% Sodium Chloride Injection for IV or IM Use (concentration = 10 mg/mL), 6 mL Syringe, Rx Only, SCA Pharmaceuticals, Windsor, CT 06095, NDC 70004-0430-09.
Quantity: 922 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