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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

Camber Pharmaceuticals Pantoprazole Sodium Tablets Recalled for Discoloration

Agency Publication Date: April 17, 2026
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Summary

Hetero Labs Limited is recalling 4,740 bottles of Pantoprazole Sodium Delayed-Release Tablets (40 mg) because the tablets may be discolored. Five consumers reported that the tablets appeared darker than normal or had light-colored spots. These prescription tablets are used to treat certain stomach and esophagus problems, such as acid reflux.

Risk

The discoloration indicates a potential change in the product's physical appearance or chemical stability, which could affect how the medication looks or works. While five complaints regarding product appearance were received, no injuries or adverse health events have been reported to date.

What You Should Do

  1. Check your prescription bottle for Pantoprazole Sodium Delayed-Release Tablets, USP, 40 mg in 1000-count bottles with NDC 31722-713-10.
  2. Verify the bottle has Batch # FD253967 and an expiration date of 06/26/2027.
  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: Pantoprazole Sodium, Delayed-Release Tablets, USP (1000-count bottle)by Camber Pharmaceuticals, Inc.
Variants: 40 mg, Delayed-Release Tablet
Lot Numbers:
FD253967 (Exp 06/26/2027)
NDC:
31722-713-10

Manufactured by Hetero Labs Limited (Unit V), India

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98671
Status: Active
Manufacturer: Hetero Labs Limited (Unit V)
Sold By: Camber Pharmaceuticals, Inc.
Manufactured In: India
Units Affected: 4,740
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.