FDA recall record

Pharmakon Pharmaceuticals Morphine Sulfate 0.5 mg/mL, Preservative Free in 0.9% Sodium recall — FDA D-0871-2016

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

Class Iclassification
D-0871-2016official record ID
Jun 1, 2016report date

Recall record at a glance

Official recordD-0871-2016
CategoryDrug Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmPharmakon Pharmaceuticals
Report dateJun 1, 2016
Recall initiation dateFeb 11, 2016
Quantity75 Syringes
LocationNoblesville, IN, United States

Official product description

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.

Why the product was recalled

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

Distribution information

IN and IL

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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