US Drug Recall Register
Class I · High risk Terminated Initiated Mar 26, 2014 (12 years ago)

Midazolam 0.2 mg/2 mL 0.9% Sodium Chloride syringes, Total dosage: 0.4 mg per 2 mL, Rx…

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

Why it was recalled

Superpotent Drug: Product contains twice the stated amount of midazolam.

What was recalled

Midazolam 0.2 mg/2 mL 0.9% Sodium Chloride syringes, Total dosage: 0.4 mg per 2 mL, Rx Only, Pharmakon Pharmaceuticals, Inc., 14450 Getz Rd, Noblesville, Indiana, NDC 45183-0014-69.

Recalling firm
Pharmakon Pharmaceuticals
NDC code
45183-0014-69
Origin
IN, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1362-2014

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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