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
Reported: December 21, 2016 Initiated: November 18, 2016 #D-0193-2017
Product Description
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
Reason for Recall
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Details
- Recalling Firm
- Cantrell Drug Company
- Units Affected
- 150 bags
- Distribution
- Nationwide
- Location
- Little Rock, AR
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Cantrell Drug Company. Units affected: 150 bags.
Why was this product recalled? ▼
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on December 21, 2016. Severity: Moderate. Recall number: D-0193-2017.
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