Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Hydromorphone Hydrochloride Injection Recalled by HOSPIRA INC, LAKE FOREST Due to Presence of Particulate Matter: Silicone oil
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, LAKE FOREST directly.
Affected Products
Hydromorphone Hydrochloride Injection, USP, 50 mg/5 mL (10 mg/mL), 5 mL Single Dose Vial.(10 vials per carton NDC 0703-0113-01) and 180 vials per case (NDC 0703-0113-03) Mfd By: Hospira, Inc., Lake Forest, IL 60045 USA, Mfd For: Teva Parenteral Medicines, Inc., Irvine, CA 92618 USA.
Quantity: 56,340 vials
Why Was This Recalled?
Presence of Particulate Matter: Silicone oil
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About HOSPIRA INC, LAKE FOREST
HOSPIRA INC, LAKE FOREST 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