US Drug Recall Register
Class I · High risk Terminated Initiated Oct 27, 2017 (9 years ago)

Midazolam Injection, USP, Preservative Free, 2 mg / 2 mL (1 mg / mL), 24 X 2mL Prefilled…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Labeling: Label MIX-UP. Blister Packages, Labeled as Midazolam injection, USP, 2 mg / 2 ml, Containing Syringes of Ondansetron Injection, USP, 4 mg / 2 mL

What was recalled

Midazolam Injection, USP, Preservative Free, 2 mg / 2 mL (1 mg / mL), 24 X 2mL Prefilled single-use syringes per carton, Rx only, Fresenius Kabi Lake Zurich, IL 60047, NDC 76045-001-20

Recalling firm
Fresenius Kabi USA, LLC
NDC code
76045-001-20
Origin
NC, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0152-2018

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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