FDA recall record

Magno Humphries Laboratories Senna Laxative (sennosides) tablets, 8.6 mg, 100-count bottles recall — FDA D-0342-2018

Labeling: Label Mix-Up: Customer complaint received that a bottle labeled as Senna Laxative contained only tablets of Naproxen Sodium 220 mg.

Class Iclassification
D-0342-2018official record ID
Feb 21, 2018report date

Recall record at a glance

Official recordD-0342-2018
CategoryDrug Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmMagno Humphries Laboratories, Inc.
Report dateFeb 21, 2018
Recall initiation dateJan 17, 2018
Quantity2,400 bottles
LocationTigard, OR, United States

Official product description

Senna Laxative (sennosides) tablets, 8.6 mg, 100-count bottles, Manufactured for: Basic Drugs, Inc., Vandalia, Ohio 45377, UPC Code 3 07610 22020 1.

Why the product was recalled

Labeling: Label Mix-Up: Customer complaint received that a bottle labeled as Senna Laxative contained only tablets of Naproxen Sodium 220 mg.

Distribution information

Nationwide in the USA

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: 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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