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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

Amerisource Health Services: Paroxetine Tablets Recalled for Presence of Foreign Tablets or Capsules

Agency Publication Date: November 21, 2017
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Summary

Amerisource Health Services is voluntarily recalling 74 cartons of Paroxetine (generic Paxil) 30mg tablets because the packaging may contain foreign tablets or capsules of a different medication. Paroxetine is a prescription antidepressant, and the presence of incorrect medications in the bottle could lead to consumers accidentally taking the wrong drug. This recall affects 100-count cartons (packaged as 10 strips of 10 unit-dose tablets) distributed nationwide by American Health Packaging.

Risk

The presence of foreign tablets or capsules means a patient may unintentionally ingest a medication other than their prescribed Paroxetine. This can lead to serious health complications, including adverse drug reactions, interactions with other medications, or a lack of treatment for the patient's underlying condition.

What You Should Do

  1. Check your medication packaging for Paroxetine Tablets, USP, 30mg (100 tablets per carton) distributed by American Health Packaging with NDC 68084-046-01.
  2. Verify if your product matches Lot 172291. You can find this lot number printed on the carton or the individual unit-dose blister strips.
  3. If you identify any foreign tablets or capsules that do not match the expected appearance of your Paroxetine medication, do not consume them.
  4. Contact your healthcare provider or pharmacist immediately for guidance if you believe you have taken the incorrect medication or to obtain a replacement prescription.
  5. Return any unused product to your pharmacy for a refund and contact Amerisource Health Services or American Health Packaging for further instructions regarding the return process.
  6. For additional questions, contact the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) or visit www.fda.gov/safety/recalls.

Your Remedy Options

๐Ÿ’ฐFull Refund
How to: Contact your healthcare provider or pharmacist for guidance. Return any unused product to the pharmacy for a refund.

Affected Products

Product: Paroxetine Tablets, USP, 30mg, 100 tablets (10 x 10)
Model:
NDC 68084-046-01
Lot Numbers:
172291

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 78490
Status: Resolved
Manufacturer: Amerisource Health Services
Sold By: American Health Packaging; Pharmacies
Manufactured In: United States
Units Affected: 74 cartons (cartons of 100 individual unit doses)
Distributed To: Nationwide

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.