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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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Medium RiskFDA Drug
Medications & Supplements/Over-the-Counter

Family Dollar OTC Drug Products Recalled for Temperature Storage Deviations

Agency Publication Date: October 16, 2023
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Summary

Family Dollar has recalled 4,261,383 units of various Over-The-Counter (OTC) drug products because they were stored outside of their required temperature limits. These products were sold at Family Dollar retail locations across 23 states. Because these medications were not kept at the correct temperatures, their quality and effectiveness cannot be guaranteed.

Risk

Medications stored outside of labeled temperature requirements can degrade or lose potency. This may result in the medicine being less effective or failing to treat the symptoms for which it was purchased.

What You Should Do

  1. This recall affects various over-the-counter (OTC) drug products sold at Family Dollar retail stores in Alabama, Arkansas, Arizona, California, Colorado, Florida, Georgia, Idaho, Kansas, Louisiana, Mississippi, Montana, North Dakota, Nebraska, New Mexico, Nevada, Oklahoma, Oregon, South Dakota, Texas, Utah, Washington, and Wyoming.
  2. Check your medication for products purchased from Family Dollar stores in these specific states. Because this recall involves over 4 million units of various products, see the Affected Products section below for the full list of affected codes.
  3. 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 Dollar Tree Distribution, Inc. directly for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls for more information.

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: Certain Over-The-Counter (OTC) drug productsby Family Dollar

Certain drug products sold by Family Dollar retail stores located in AL, AR, AZ, CA, CO, FL, GA, ID, KS, LA, MS, MT, ND, NE, NM, NV, OK, OR, SD, TX, UT, WA, and WY. Recall number D-0045-2024.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93187
Status: Active
Manufacturer: Dollar Tree Distribution, Inc.
Sold By: Family Dollar
Manufactured In: United States
Units Affected: 4,261,383 units of various products
Distributed To: Alabama, Arkansas, Arizona, California, Colorado, Florida, Georgia, Idaho, Kansas, Louisiana, Mississippi, Montana, North Dakota, Nebraska, New Mexico, Nevada, Oklahoma, Oregon, South Dakota, Texas, Utah, Washington, Wyoming

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 FDA Press Release 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.