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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/Over-the-Counter

AAA Pharmaceutical, Inc.: Allergy Relief Fexofenadine Tablets Recalled for Missing Lot or Expiration Dates

Agency Publication Date: March 4, 2020
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Summary

AAA Pharmaceutical, Inc. is recalling 3,456 bottles of Discount Drug Mart Allergy Relief (fexofenadine hydrochloride) tablets because the labels may be missing or have incorrect lot numbers and expiration dates. This recall affects the 180 mg strength 24-hour antihistamine tablets sold in both 30-count and 45-count bottles. These products were distributed to Discount Drug Mart locations specifically within Ohio. Because the lot and expiration information is critical for tracking shelf life and safety, consumers are advised to check their medication to see if it belongs to the affected batches.

Risk

Incorrect or missing expiration dates and lot numbers prevent consumers and the manufacturer from knowing if the medication is still safe or effective. Using medication past its expiration date may lead to decreased potency, meaning the antihistamine may not effectively treat allergy symptoms as intended.

What You Should Do

  1. Check your medicine cabinet for 'Discount Drug Mart Allergy Relief' (fexofenadine hydrochloride) 180 mg tablets in 30-count or 45-count bottles.
  2. Verify the UPC and NDC codes on the packaging. Affected 30-count bottles have NDC 53943-192-04 and UPC 0-93351-03069-7. Affected 45-count bottles have NDC 53943-192-06 and UPC 0-93351-03070-3.
  3. Inspect the label for the following lot numbers and expiration dates: Lot P138855 (Exp. 05/30/2022) for 30-count bottles, or Lot P138856 (Exp. 05/30/2022) for 45-count bottles.
  4. If your bottle matches these lot numbers or is missing clear lot/expiration information, stop using the medication and contact your healthcare provider or pharmacist for guidance.
  5. Return any unused product to the Discount Drug Mart or Drug Mart Food Fair location where it was purchased for a full refund.
  6. For questions about this recall, you can contact the FDA Consumer Complaint hotline at 1-888-723-3332 or visit www.fda.gov/safety/recalls.

Your Remedy Options

๐Ÿ’ฐFull Refund

Full refund upon return.

How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund.

Affected Products

Product: Discount Drug Mart Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg (30 tablets)
Model:
NDC 53943-192-04
UPC Codes:
093351030697
Lot Numbers:
P138855 (Exp. 05/30/2022)
Date Ranges: 05/30/2022
Product: Discount Drug Mart Allergy Relief, Fexofenadine Hydrochloride Tablets, 180 mg (45 tablets)
Model:
NDC 53943-192-06
UPC Codes:
093351030703
Lot Numbers:
P138856 (Exp. 05/30/2022)
Date Ranges: 05/30/2022

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 84938
Status: Resolved
Manufacturer: AAA Pharmaceutical, Inc.
Sold By: Discount Drug Mart; Drug Mart - Food Fair
Manufactured In: United States
Units Affected: 3456 Bottles
Distributed To: Ohio

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.