HOSPIRA INC, LAKE FOREST recalls Hydromorphone Hydrochloride Injection, USP, 500 mg/50 mL (10
See all recalls from HOSPIRA INC, LAKE FOREST →Recalled Product
Hydromorphone Hydrochloride Injection, USP, 500 mg/50 mL (10 mg/mL), 50 mL Single Dose Vial. Mfd For: Teva Parenteral Medicines, Inc., Irvine, CA 92618 USA. NDC: 0703-0018-01
Hazard / Issue
Presence of Particulate Matter: Silicone oil
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot #: 560053F, 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.
Looking for a safe alternative?
Search Amazon for Hydromorphone Hydrochloride Injection, USP, →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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