FDA recall record

Testosterone Topical Solution 30mg of testosterone per pump actuation * each actuation recall — FDA D-1454-2019

Defective Container; actuator may improperly function and affect dose delivery.

Class IIIclassification
D-1454-2019official record ID
Jul 10, 2019report date

Recall record at a glance

Official recordD-1454-2019
CategoryDrug Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmInvaGen Pharmaceuticals, Inc.
Report dateJul 10, 2019
Recall initiation dateJun 12, 2019
Quantity1776 bottles
LocationCentral Islip, NY, United States

Official product description

Testosterone Topical Solution 30mg of testosterone per pump actuation * each actuation delivers 1.5 mL of solution Total contents: 110 mL to deliver 90 mL, Manufactured by: Cipla Ltd, Verna Goa, India Manufactured for: Cipla USA, Inc., Sunrise, FL 33323 NDC 69097-363-44

Why the product was recalled

Defective Container; actuator may improperly function and affect dose delivery.

Distribution information

Nationwide

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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