HOSPIRA INC, LAKE FOREST recalls Hydromorphone Hydrochloride Injection, USP, 50 mg/5 mL (10 m
See all recalls from HOSPIRA INC, LAKE FOREST →Recalled Product
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.
Hazard / Issue
Presence of Particulate Matter: Silicone oil
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot #: 560103F, Exp. 01AUG2017
✅ What Should You Do?
- 1Stop taking this medication and contact your doctor or pharmacist immediately.
- 2Do NOT flush medications down the drain — use an FDA-approved drug take-back program.
- 3Check the lot number on your bottle or packaging against the recalled lots listed above.
- 4Report adverse events to FDA MedWatch or call 1-800-FDA-1088.
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