Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class I · High risk Terminated Initiated Mar 26, 2014 (13 years ago)

Midazolam 0.2 mg/2 mL 0.9% Sodium Chloride syringes

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.

Cause type: Wrong potency / content

Sub- or super-potent product, or a failed content-uniformity / assay test. You may receive too little or too much active ingredient - a direct dosing risk. All wrong potency / content recalls.

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.

Affected NDC 45183-0014-69

Compare with the code on your package — it is the most precise check available.

Drug: Midazolam

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

Treat this as urgent. Class I means FDA judged there is a reasonable probability of serious harm. Find the lot number on your package; if it matches the recalled lots, do not take another dose before you have spoken to your pharmacist or prescriber - today, not next week. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

Other Midazolam recalls

See all
Class II · Moderate risk

midazolam in dextrose 5%

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

Terminated Sterility / contamination Central Admixture Pharmacy Services Inc NDC 71286-4036-1 D-1075-2023
Class II · Moderate risk

Midazolam Injection

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

Ongoing Stability / shelf life Akorn, Inc. D-0859-2023

Other recalls by Pharmakon Pharmaceuticals

All 2014 recalls