US Drug Recall Register
Class II · Moderate risk Terminated Initiated Apr 12, 2016 (10 years ago)

Brevibloc DOUBLE STRENGTH Premixed Injection, Esmolol Hydrochloride in Sodium Chloride…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Discoloration: presence of atypical yellow discoloration of the solution .

What was recalled

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

Recalling firm
Baxter Healthcare Corp.
NDC code
10019-075-87
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0852-2016

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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