Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
KETOROLAC Tromethamine Inj. Recalled by Hospira Inc. Due to Crystallization; identified as calcium salt of Ketorolac
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
KETOROLAC Tromethamine Inj., USP, 30 mg (30 mg/mL), 1 mL Fill, Single-dose Vials, I.V/I.M. USE, Hospira, Inc., Lake Forest, IL 60045 --- NDC 0409-3795-01 --- Also labeled under NOVAPLUS label NDC 0409-3795-49
Quantity: 12,460,975 vials(Hospira label); 3,016,500 vials (NOVAPLUS label)
Why Was This Recalled?
Crystallization; identified as calcium salt of Ketorolac
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