Perrigo New York, Inc. recalls Ciclopirox shampoo 1%,120 mL bottle, Rx only, Manufactured By Perrigo Bronx, NY 10457 Distributed by Perrigo Allegan,
Perrigo recalls 1% Ciclopirox shampoo bottles with impurities found during stability testing. Rx-only product may pose safety risks if not properly handled.
Lower-risk recall
Failed Degradation/Impurities Specifications: Out of specification related substance results during stability testing.
Contact the company & request your remedy
What happened, in plain English
Perrigo is recalling 1% Ciclopirox shampoo bottles that tested with impurities during stability checks. This could pose safety risks if the product is used as directed. Read more at govinfonow.com/recall/39191-perrigo-ciclopirox-shampoo-recall-impurities-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/39191-perrigo-ciclopirox-shampoo-recall-impurities-risk · Updated October 5, 2026 · FDA enforcement record: FDA #D-0512-2019
Cite this page
“Perrigo Ciclopirox Shampoo Recall: Impurities Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/39191-perrigo-ciclopirox-shampoo-recall-impurities-risk. Based on FDA recall #D-0512-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0512-2019%22&limit=1).
Why it’s dangerous
The shampoo contains impurities that didn't meet safety standards during testing. These impurities could potentially cause skin irritation or other adverse reactions if used improperly.
Who’s affected
People with a prescription for Ciclopirox shampoo who received bottles with lot numbers 7DT0280 or 7ET0565 from the specified manufacturers. Those using the product for fungal infections are most at risk.
How to tell if you have this one
Check for the product name 'Ciclopirox shampoo 1%', 120 mL bottle, prescription-only. Look for lot numbers 7DT0280 or 7ET0565 on the label.
- Brand
Perrigo- Category
Drug
What to do — step by step
Check Product Label
Look for lot numbers 7DT0280 or 7ET0565 on the bottle label.
Questions people ask
Is this shampoo safe to use?
The recall indicates impurities were found during testing, but the product may still be safe for use if handled properly. Consult your doctor for guidance.
What should I do if I have this product?
The recall record does not specify a remedy, so contact your doctor or pharmacist for advice.
How can I tell if I have the recalled product?
Check for lot numbers 7DT0280 or 7ET0565 on the bottle label.
Contact Perrigo
We’ve drafted a message you can send Perrigo to request your refund or repair — edit it as you like.
Subject: Recall D-0512-2019 — Perrigo Perrigo Hello, I own a Perrigo that is covered by recall D-0512-2019 from Perrigo. 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-0512-2019 (February 13, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0512-2019 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.