Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ketamine inj 50 mg per 1 mL Recalled by Hikma Injectables USA Inc Due to Lack of Assurance of Sterility: The tamper-evident seal...
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 Hikma Injectables USA Inc directly.
Affected Products
ketamine inj 50 mg per 1 mL, Rx Only, 1 mL fill in a 3mL pre-filled syringe, For IV or IM Use, Hikma Injectables USA Inc., 36 Stults Road, Dayton, NJ 08810, This is a Compounded Drug. Hospital/Office Use Only. NDC 63037-137-25
Quantity: 1,800 syringes
Why Was This Recalled?
Lack of Assurance of Sterility: The tamper-evident seal on several of the syringes are not attached upon receipt of shipment.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Hikma Injectables USA Inc
Hikma Injectables USA Inc has 4 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report