Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Heparin Sodium Recalled by Cantrell Drug Company Due to Lack of Assurance of Sterility - the firm...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Cantrell Drug Company directly.
Affected Products
Heparin Sodium, 1 USP Unit/2 mL (0.5 USP Units/mL) in 0.45% Sodium Chloride, Single-Dose Syringe, Hospital/Office Use Only, Rx Only, Cantrell Drug Co. 7321 Cantrell Rd. Little Rock, AR 72207, NDC 52533-148-16
Quantity: 1494 syringes
Why Was This Recalled?
Lack of Assurance of Sterility - the firm is recalling select sterile drug products.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Cantrell Drug Company
Cantrell Drug Company has 52 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report