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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/Prescription Drugs

RemedyRepack Inc.: Carvedilol 25 mg Tablets Recalled for Potential Paroxetine Contamination

Agency Publication Date: August 20, 2021
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Summary

RemedyRepack Inc. has recalled 4 bottles of Carvedilol 25 mg tablets (generic Coreg), a medication used to treat high blood pressure and heart failure. The recall was initiated because a 500-count source bottle was found to contain two tablets of Paroxetine 40 mg (generic Paxil), an antidepressant, which were then repackaged into 180-count bottles. Consumers should contact their healthcare provider or pharmacist immediately if they have this medication, as taking the wrong drug can lead to unintended side effects or lack of treatment for their primary condition.

Risk

Patients may inadvertently ingest Paroxetine instead of Carvedilol, which could lead to adverse drug reactions or the sudden loss of blood pressure management.

What You Should Do

  1. Check your prescription bottle for 'Carvedilol 25 mg' repackaged by RemedyRepack Inc. with NDC 70518-1826-01.
  2. Look for Lot # B1273286-071521 with an expiration date of 07/31/2022 on the label.
  3. If your bottle matches this lot number, contact your healthcare provider or pharmacist immediately for guidance and to obtain a replacement.
  4. Return any unused product from the affected lot to the pharmacy where you received it for a refund.
  5. Contact RemedyRepack Inc. for further instructions regarding this recall.
  6. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions.

Your Remedy Options

๐Ÿ’ฐFull Refund

Healthcare provider consultation and pharmacy refund

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

Affected Products

Product: Carvedilol 25 mg, 180-count bottle
Model:
NDC 68382-0095-05
NDC 70518-1826-01
Lot Numbers:
B1273286-071521 (Exp 07/31/2022)
Date Ranges: 07/31/2022

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 88536
Status: Resolved
Manufacturer: RemedyRepack Inc.
Sold By: medical facilities
Manufactured In: United States
Units Affected: 4
Distributed To: Virginia, Florida

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 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.