FDA recall record

Pharmedium Services Morphine Sulfate, 2 mg per mL (60 mg per 30 mL) 30 mL total volume in a recall — FDA D-0658-2016

Sub-potent Drug; firm's analysis revealed subpotent result for morphine sulfate assay.

Class Iclassification
D-0658-2016official record ID
Feb 17, 2016report date

Recall record at a glance

Official recordD-0658-2016
CategoryDrug Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmPharmedium Services, LLC
Report dateFeb 17, 2016
Recall initiation dateMay 22, 2015
Quantity19 Syringes
LocationLake Forest, IL, United States

Official product description

Morphine Sulfate, 2 mg per mL (60 mg per 30 mL) 30 mL total volume in a 35 mL Monoject Barrel Syringes in Sodium Chloride 0.9%, Rx only, Contains Sulfites, Compounded Drug, Not for Resale, Hospital/Office Use only, IV use only, NDC 61553-401-44.

Why the product was recalled

Sub-potent Drug; firm's analysis revealed subpotent result for morphine sulfate assay.

Distribution information

WI

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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