Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
Ceftazidime for Injection USP and Dextrose for Injection USP Recalled by B. Braun Medical Inc Due to Failed Stability Specifications: Out-of-Specification (OOS) results for High...
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
Ceftazidime for Injection USP and Dextrose for Injection USP, 2 g, 50 mL Duplex Container, RX only, B Braun Medical Inc., Bethlehem, PA 18018-3524, NDC 0264-3145-11
Quantity: 22,488 Duplex containers
Why Was This Recalled?
Failed Stability Specifications: Out-of-Specification (OOS) results for High Molecular Weight Polymers.
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