Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Ketamine Injection Recalled by Apollo Care, 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 Apollo Care, LLC directly.
Affected Products
Ketamine Injection, 50 mg per 5 mL (10 mg/mL), Single-Use Syringe, Rx only, Apollo Care, LLC, 3801 Mojave Ct., Suite 101, Columbia, MO 65202. NDC 71170-050-05
Quantity: 2040 syringes
Why Was This Recalled?
Lack of Assurance of Sterility
Where Was This Sold?
Missouri only
About Apollo Care, LLC
Apollo Care, LLC has 17 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report