FDAFDA · Food and drugs·Recall number D-1082-2017
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.
Published August 16, 2017 · Recall initiated: July 26, 2017
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Presence of Particulate Matter: Silicone oil
What to do
Voluntary: Firm initiated · Telephone
Recall details
- Brand
- HYDROMORPHONE HYDROCHLORIDE
- Manufacturer
- HOSPIRA INC, LAKE FOREST
- Distributor
- Nationwide in the USA
- UPC
- 0307030110038
- Lot
- Lot #: 560103F, Exp. 01AUG2017
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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