US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jun 19, 2019 (7 years ago)

Midazolam 1mg/Ml in Nacl 0.9% Inj Sol Syr

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

Why it was recalled

Lack of Assurance of Sterility

What was recalled

MIDAZOLAM 1MG/ML IN NACL 0.9% INJ SOL SYR (C-IV), 10 ML per syringe, RXQ Compounding, 340 West State Street, Unit 9, Athens, OH 45701. NDC: 70731-0135-86

Recalling firm
RXQ Compounding LLC
Origin
OH, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1682-2019

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.

Other Midazolam recalls

See all
Class II · Moderate risk Terminated

midazolam in dextrose 5%

Reason Lack of assurance of sterility:

Central Admixture Pharmacy Services Inc NDC 71286-4036-1 D-0018-2024
Class II · Moderate risk Terminated

midazolam in dextrose 5%

Reason Lack of assurance of sterility: Lack of validation data for sanitization cycles

Central Admixture Pharmacy Services Inc NDC 71286-4036-1 D-1075-2023
Class II · Moderate risk Ongoing

Midazolam Injection

Reason CGMP Deviations: Firm went out of business and could no longer continue stability studies.

Akorn, Inc. D-0859-2023