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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/Prescription Drugs

Rising Pharma Pregabalin Capsules Recalled for Presence of Foreign Tablet

Agency Publication Date: June 4, 2024
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Summary

Rising Pharma Holdings, Inc. has recalled one lot of Pregabalin Capsules 50mg, sold in 1000-count bottles, which is a prescription medication used to treat nerve pain and seizures. The recall was issued after a foreign tablet, identified as the acid reflux medication pantoprazole 20mg, was discovered inside a bottle during the packaging process. If you have any health concerns or believe you have taken the wrong medication, contact your healthcare provider or pharmacist immediately.

Risk

Taking a foreign tablet instead of the prescribed medication could lead to a lack of treatment for the intended condition or potential side effects from the unintended drug. No injuries or adverse events have been reported to date.

What You Should Do

  1. This recall affects Rising Pharma Pregabalin Capsules 50mg in 1000-count bottles with NDC 64980-411-10, Lot 23132611, and an expiration date of 07/31/2026.
  2. 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 Rising Pharma Holding, Inc. for further instructions.
  3. 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: Pregabalin Capsules 50mg (1000-count bottle)by Rising Pharma Holdings, Inc.
Variants: 50mg, 1000-count, Capsule
Lot Numbers:
23132611 (Exp 07/31/2026)
NDC:
64980-411-10

Recall due to discovery of a single pantoprazole 20mg tablet in a bottle.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 94642
Status: Active
Manufacturer: Rising Pharma Holding, Inc.
Sold By: Pharmacies; Healthcare facilities
Manufactured In: India
Distributed To: Nationwide

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.