FDA recall record

Morphine Sulfate Oral Solution, 100 mg/ 5 mL (20 mg/mL) recall — FDA D-1126-2017

Defective container: Oral solution leaking from container.

Class IIclassification
D-1126-2017official record ID
Sep 6, 2017report date

Recall record at a glance

Official recordD-1126-2017
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmTris Pharma Inc.
Report dateSep 6, 2017
Recall initiation dateJun 15, 2017
Quantity34,824 bottles
LocationMonmouth Junction, NJ, United States

Official product description

Morphine Sulfate Oral Solution, 100 mg/ 5 mL (20 mg/mL), packaged in a 1 oz. bottle containing 30 mL with an oral syringe, Rx Only, Manufactured by: Tris Pharma, Inc. Monmouth Junction, NJ 08852, NDC 27808-082-01

Why the product was recalled

Defective container: Oral solution leaking from container.

Distribution information

U.S.A. Nationwide

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

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

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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