FDAFDA · Food and drugs·Recall number D-0193-2017
Heparin Sodium 5,000 USP Units Added to 0.9% Sodium Chloride 1,000 mL* Bag (5 USP units/mL), Single-Dose Bag.,Hospital/Office Use Only, Injection Solution For IV Use, Rx Only, Cantrell Drug Company 7321 Cantrell Road Little Rock, AR 72207, NDC 52533-097-24
Published December 21, 2016 · Recall initiated: November 18, 2016
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
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
What to do
Voluntary: Firm initiated · Press Release
Recall details
- Manufacturer
- Cantrell Drug Company
- Distributor
- Nationwide
- Lot
- Lot: 167081
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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