FDA recall record

Testosterone Topical Solution, 30mg/1.5mL, 110mL bottles recall — FDA D-0087-2019

Defective Container: Repetitive complaints received indicating pump not working.

Class IIIclassification
D-0087-2019official record ID
Oct 31, 2018report date

Recall record at a glance

Official recordD-0087-2019
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmLupin Pharmaceuticals Inc.
Report dateOct 31, 2018
Recall initiation dateOct 9, 2018
Quantity6,752 bottles
LocationBaltimore, MD, United States

Official product description

Testosterone Topical Solution, 30mg/1.5mL, 110mL bottles, Rx only, Manufactured for: Lupin Pharmaceuticals Inc. Baltimore, Maryland 21202 United States, Manufactured by: Lupin Limited Pithampur (M.P.) 454 775 INDIA, NDC 68180-943-11

Why the product was recalled

Defective Container: Repetitive complaints received indicating pump not working.

Distribution information

Nationwide within the United States

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken 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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