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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

Espumil Lipophilic Foam Base Recalled for Labeling Errors

Agency Publication Date: October 29, 2025
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Summary

Letco Medical LLC is recalling 173 bottles of Espumil Lipophilic foam base, a pharmaceutical compounding product used in topical medications. The recall was initiated because the product labeling is incorrect or missing necessary information. Approximately 173 bottles were distributed to 44 compounding pharmacies and two distributors primarily located in Alabama and surrounding areas.

Risk

The labeling error could lead to improper use or handling of the foam base by compounding pharmacists, potentially resulting in incorrectly formulated medications for patients. No injuries have been reported to date.

What You Should Do

  1. Check your supply for 500 ml bottles of Espumil Lipophilic foam base with Batch # 24G15-T02-115604 and an expiration date of 11/30/2026.
  2. If you have health concerns, contact your healthcare provider or pharmacist. Return any unused product to the place of purchase for a refund, throw it away, or contact Letco Medical LLC for further instructions.
  3. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Contact your healthcare provider or pharmacist for guidance, or return any unused product to the place of purchase for a refund
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away. For prescription medications, a DEA take-back location or pharmacy mail-back program is preferred when available.

Affected Products

Product: Espumil, Lipophilic foam base (500 ml)by Espumil
Variants: Lipophilic foam base
Lot Numbers:
24G15-T02-115604 (Exp 11/30/2026)

Recall #: D-0138-2026; Quantity: 173 bottles

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97660
Status: Active
Manufacturer: Letco Medical LLC
Sold By: Compounding pharmacies; Distributors
Manufactured In: United States
Units Affected: 173 500 ml bottles
Distributed To: Alabama

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.