Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Ketamine Hydrochloride Injection Recalled by Hospira Inc. Due to Defective Container: There were customer complaints of cracked...
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 Hospira Inc. directly.
Affected Products
Ketamine Hydrochloride Injection, USP (100 mg/mL) packaged in 5 mL multi-dose glass fliptop vials, 10 vials per box, Rx only, Manufactured by: Hospira Inc., Lake Forest, IL 60045. NDC 00409-2051-05
Quantity: 83,320 vials
Why Was This Recalled?
Defective Container: There were customer complaints of cracked and leaking glass vials.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Hospira Inc.
Hospira Inc. has 245 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report