Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Heparin Sodium Recalled by B. Braun Medical Inc Due to Subpotent: Low anti-factor IIa Potency.
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 B. Braun Medical Inc directly.
Affected Products
Heparin Sodium, 25,000 USP units per 250mL, (100 USP units per mL) in 5% Dextrose injection, 250 ml Excel Container, B. Braun Medical Inc. Bethlehem, PA 18018, USA; API from Spain NDC: 0264-9587-20,
Quantity: 1,380
Why Was This Recalled?
Subpotent: Low anti-factor IIa Potency.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About B. Braun Medical Inc
B. Braun Medical Inc has 25 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report