Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Brevibloc DOUBLE STRENGTH Premixed Injection Recalled by Baxter Healthcare Corp. Due to Discoloration: presence of atypical yellow discoloration of the...
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 Baxter Healthcare Corp. directly.
Affected Products
Brevibloc DOUBLE STRENGTH Premixed Injection, Esmolol Hydrochloride in Sodium Chloride, 2000mg/100mL (20 mg/mL), 100 mL, Rx only, Manufactured by Baxter Healthcare Corporation, Deerfield, Il 60015, NDC 10019-075-87
Quantity: 11,630 babs
Why Was This Recalled?
Discoloration: presence of atypical yellow discoloration of the solution .
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Baxter Healthcare Corp.
Baxter Healthcare Corp. has 126 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report