Lupin Pharmaceuticals Inc. recalls Testosterone Topical Solution, 30mg/1.5mL, 110mL bottles, Rx only, Manufactured for: Lupin Pharmaceuticals Inc.
Lupin Pharmaceuticals recalls 30mg/1.5mL testosterone topical solution bottles due to pump malfunction. This affects Rx-only products with specific lot numbers and manufacturing dates.
Lower-risk recall
Defective Container: Repetitive complaints received indicating pump not working.
Contact the company & request your remedy
What happened, in plain English
Lupin Pharmaceuticals is recalling testosterone topical solution bottles that have a pump that doesn't work properly. This could lead to incorrect dosing if the product is used without the pump functioning correctly. Read more at govinfonow.com/recall/39090-lupin-testosterone-topical-solution-recall-pump-not-working.
Source Summary by GovInfoNow · govinfonow.com/recall/39090-lupin-testosterone-topical-solution-recall-pump-not-working · Updated October 5, 2026 · FDA enforcement record: FDA #D-1010-2019
Cite this page
“Lupin Testosterone Topical Solution Recall: Pump Not Working.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/39090-lupin-testosterone-topical-solution-recall-pump-not-working. Based on FDA recall #D-1010-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1010-2019%22&limit=1).
Why it’s dangerous
The pump in the testosterone solution bottle is defective and doesn't work properly. This means users might not get the correct dose of testosterone if they try to use the product without the pump functioning.
Who’s affected
People with prescriptions for testosterone topical solution who received this specific product. Those using the product without the pump working may be at risk of incorrect dosing.
How to tell if you have this one
Check for bottles labeled 'Testosterone Topical Solution, 30mg/1.5mL, 110mL' with the NDC code 68180-943-11. The product was manufactured for Lot # K700086 and expired November 2019.
- Brand
Lupin Pharmaceuticals- Category
Drug
What to do — step by step
Check Product Details
Look for the NDC code 68180-943-11 on the bottle label to confirm it's part of this recall.
Questions people ask
Is this product safe to use?
The recall indicates the pump may not work properly, which could lead to incorrect dosing. The product is not safe to use as intended without the pump functioning correctly.
What should I do if I have this product?
The recall does not specify a remedy, so contact Lupin Pharmaceuticals for guidance on next steps.
How can I tell if I have the recalled product?
Check for the NDC code 68180-943-11 and the lot number K700086 on the bottle label.
Contact Lupin Pharmaceuticals
We’ve drafted a message you can send Lupin Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-1010-2019 — Lupin Pharmaceuticals Lupin Pharmaceuticals Hello, I own a Lupin Pharmaceuticals that is covered by recall D-1010-2019 from Lupin Pharmaceuticals. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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-1010-2019 (March 13, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1010-2019 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 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.