Lupin Recalls Testosterone Topical Solution Due to Defective Pump
Lupin Pharmaceuticals recalls specific lots of Testosterone Topical Solution because the pump may not work. Check your bottle's lot number and expiration date.
Use caution until it’s fixed
Defective Container: Repetitive complaints received indicating pump not working.
Contact the company
What happened, in plain English
Lupin Pharmaceuticals Inc. has recalled 6,752 bottles of Testosterone Topical Solution (30mg/1.5mL) due to a defective container issue. The recall was initiated after receiving repetitive complaints that the pump mechanism on the bottles was not working properly. This defect prevents users from dispensing the medication as intended. Read more at govinfonow.com/recall/39511-lupin-recalls-testosterone-topical-solution-due-to-defective-pump.
Source Summary by GovInfoNow · govinfonow.com/recall/39511-lupin-recalls-testosterone-topical-solution-due-to-defective-pump · Updated October 11, 2026 · FDA enforcement record: FDA #D-0087-2019
Cite this page
“Lupin Recalls Testosterone Topical Solution Due to Defective Pump.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/39511-lupin-recalls-testosterone-topical-solution-due-to-defective-pump. Based on FDA recall #D-0087-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0087-2019%22&limit=1).
Why it’s dangerous
The primary hazard is a defective container where the pump fails to function. This does not pose a direct physical injury risk like fire or laceration, but it renders the product unusable, potentially leading to missed doses of necessary medication.
Who’s affected
Individuals who have purchased Testosterone Topical Solution manufactured by Lupin Pharmaceuticals Inc. between the relevant production dates and before the expiration of November 2019. These are likely patients prescribed this specific Rx medication for testosterone replacement therapy.
How to tell if you have this one
Look for 110mL bottles of Testosterone Topical Solution, Rx only, manufactured by Lupin Pharmaceuticals Inc. in Baltimore, Maryland. Check the label for NDC 68180-943-11 and lot numbers K700085 or K700087 with an expiration date of November 2019.
- Brand
Lupin Pharmaceuticals- Category
Drug
What to do — step by step
Check Your Bottle
Verify if your bottle matches the recalled NDC 68180-943-11 and lot numbers K700085 or K700087.
Contact Your Pharmacist
If you have the recalled product, contact your pharmacy or healthcare provider to discuss replacement options since no specific remedy is listed in the record.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide within the United States” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 14 months after the firm started it.
- Firm started the recall
- FDA classified it Class III
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
Questions people ask
How many bottles are being recalled?
A total of 6,752 bottles are included in this recall.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-0087-2019 (October 9, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0087-2019 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 11, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.