Reported Aug 16, 2017 · Terminated
Hydromorphone Hydrochloride Injection, USP, 50 mg/5 mL (10 mg/mL), 5 mL Single Dose Vial.(10 vials per carton NDC…
Hospira Inc., Lake Forest
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: HOSPIRA INC, LAKE FOREST · 275 NORTH FOREST DRIVE · LAKE FOREST, IL · 60045
Is this the product you have?
- 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 ByHospira, Inc., Lake Forest, IL 60045 USA
- Mfd ForTeva Parenteral Medicines, Inc., Irvine, CA 92618 USA
- Lot codes and dates
Lot #: 560103FExp. 01AUG2017
- Amount recalled
- 56,340 vials
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
- Nationwide
Why it was recalled
Presence of Particulate Matter: Silicone oil
This product could cause temporary or reversible health problems — stop using it.
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