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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Low RiskFDA Drug
Medications & Supplements/Topical Products

Lupin Pharmaceuticals Inc.: Testosterone Topical Solution Recalled Due to Defective Pump

Agency Publication Date: October 23, 2018
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Summary

Lupin Pharmaceuticals Inc. has recalled 6,752 bottles of Testosterone Topical Solution (30mg/1.5mL) because the delivery pump may not function correctly. This recall affects 110mL bottles distributed nationwide within the United States. Patients using this medication have reported repetitive issues with the pump failing to work, which can prevent them from receiving their prescribed dose of medication. If you have this product, you should contact your doctor or pharmacist to discuss your treatment and how to obtain a replacement.

Risk

The defective pump prevents the bottle from dispensing the medication as intended. This failure may lead to patients missing doses or receiving an inconsistent amount of the testosterone replacement therapy, potentially causing a recurrence of symptoms associated with low testosterone.

What You Should Do

  1. Check your bottle of Testosterone Topical Solution (30mg/1.5mL) for lot numbers K700085 or K700087 and expiration date November 2019.
  2. Verify the National Drug Code (NDC) on the label is 68180-943-11 to confirm if your 110mL bottle is part of this recall.
  3. Contact your healthcare provider or pharmacist immediately to report the defective pump and discuss continued treatment options.
  4. Return any unused or defective product to the pharmacy where you purchased it for a refund or instructions on disposal.
  5. Contact Lupin Pharmaceuticals Inc. directly for further information regarding this recall or for guidance on replacement units.
  6. For additional questions or to report adverse events, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

๐Ÿ’ฐFull Refund

Healthcare provider consultation and pharmacy return

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund

Affected Products

Product: Testosterone Topical Solution (110mL)
Model:
NDC 68180-943-11
Recall #: D-0087-2019
Lot Numbers:
K700085 (Exp. November 2019)
K700087 (Exp. November 2019)
Date Ranges: Exp. November 2019

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 81213
Status: Resolved
Manufacturer: Lupin Pharmaceuticals Inc.
Sold By: pharmacies
Manufactured In: India, United States
Units Affected: 6,752 bottles
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.