US Drug Recall Register
Class I · High risk Terminated Initiated Feb 11, 2016 (11 years ago)

Morphine Sulfate 0.5 mg/mL, Preservative Free in 0.9% Sodium Chloride, Rx, total volume…

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

Why it was recalled

Super-Potent Drug: Out of specification for potency results (high) were obtained for one lot of morphine sulfate Inj.

What was recalled

Morphine Sulfate 0.5 mg/mL, Preservative Free in 0.9% Sodium Chloride, Rx, total volume 1 mL, This is a compounded drug, CII, IV Use, syringe, Pharmakon Pharmaceuticals, NDC 45183-0322-78.

Recalling firm
Pharmakon Pharmaceuticals
NDC code
45183-0322-78
Origin
IN, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0871-2016

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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