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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

Rising Pharma Bupropion XL 150mg Tablets Recalled for Foreign Medication

Agency Publication Date: January 11, 2024
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Summary

Rising Pharma Holding, Inc. is recalling 47,976 bottles of buPROPion Hydrochloride Extended-Release Tablets, USP (XL) 150mg, a prescription medication used to treat depression. The recall was issued because foreign tablets or capsules from a different medication were found inside the 30-count bottles. No injuries or medical incidents have been reported to date regarding this issue.

Risk

Ingesting an incorrect medication from a prescription bottle could cause a patient to experience unintended side effects or fail to receive the therapeutic benefits of their prescribed treatment. Patients may be at risk if they consume a foreign tablet or capsule that was mistakenly packaged in the bottle.

What You Should Do

  1. This recall affects 30-count bottles of buPROPion Hydrochloride Extended-Release Tablets, USP (XL) 150mg (NDC 16571-862-03) manufactured for Rising Pharma Holdings, Inc.
  2. Check the bottle label for lot number BPA123098A with an expiration date of 06/2025.
  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 the manufacturer for further instructions.
  4. 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: buPROPion Hydrochloride Extended-Release Tablets, USP (XL) 150mg (30-count bottle)by Rising Pharma Holdings, Inc.
Variants: 150mg, Extended-Release (XL), 30-count bottle, Tablet, Rx Only
Lot Numbers:
BPA123098A (Exp. Date 06/2025)
NDC:
16571-862-03

Manufactured by Graviti Pharmaceuticals Pvt. Ltd. in Telangana, India.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93706
Status: Active
Manufacturer: Rising Pharma Holding, Inc.
Sold By: pharmacies
Manufactured In: India, United States
Units Affected: 47,976 bottles
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.