Jubilant Recalls Pantoprazole Tablets Due to Manufacturing Deviations
Jubilant Cadista recalls 12,770 bottles of Pantoprazole Sodium 40mg tablets due to cGMP deviations. Check your lot numbers and expiration dates.
Use caution until it’s fixed
cGMP Deviations: Oral products were not manufactured in accordance with Good Manufacturing Practices.
Contact the company
What happened, in plain English
Jubilant Cadista Pharmaceuticals Inc. is recalling 12,770 bottles of Pantoprazole Sodium Delayed Release Tablets USP, 40 mg because they were not manufactured in accordance with current Good Manufacturing Practices (cGMP). The affected products are distributed nationwide and include specific lot numbers with expiration dates in May 2014. No remedy or return instructions are currently stated in the record. Read more at govinfonow.com/recall/48345-jubilant-cadista-pharmaceuticals-inc-recalls-pantoprazole-sodium-delayed-release-tablets.
Source Summary by GovInfoNow · govinfonow.com/recall/48345-jubilant-cadista-pharmaceuticals-inc-recalls-pantoprazole-sodium-delayed-release-tablets · Updated October 13, 2026 · FDA enforcement record: FDA #D-296-2013
Cite this page
“Jubilant Recalls Pantoprazole Tablets Due to Manufacturing Deviations.” GovInfoNow, updated October 13, 2026. https://govinfonow.com/recall/48345-jubilant-cadista-pharmaceuticals-inc-recalls-pantoprazole-sodium-delayed-release-tablets. Based on FDA recall #D-296-2013 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-296-2013%22&limit=1).
Why it’s dangerous
The hazard stems from cGMP deviations, meaning the oral products were not manufactured in accordance with Good Manufacturing Practices. This can lead to inconsistencies in drug strength, purity, or contamination, potentially affecting the medication's safety and efficacy.
Who’s affected
Consumers who purchased Pantoprazole Sodium Delayed Release Tablets USP, 40 mg from nationwide distributors between the time of manufacture and the recall date. Individuals relying on these specific batches for acid reduction or related conditions are most at risk due to potential quality control failures.
How to tell if you have this one
Check your bottle for NDC 59746-284-90. Look for Lot numbers PA22028 or PA22029 with an expiration date of 5/2014. The product is marketed by Jubilant Cadista Pharmaceutical Inc in Salisbury, MD, and manufactured by Jubilant Life Sciences Ltd in India.
- Brand
Jubilant Cadista Pharmaceuticals- Category
Drug
What to do — step by step
Check Your Bottle
Verify if your Pantoprazole Sodium bottle has NDC 59746-284-90 and Lot numbers PA22028 or PA22029 with an expiration date of 5/2014.
Contact Manufacturer
Since no remedy is stated, contact Jubilant Cadista Pharmaceuticals Inc. directly for further instructions on what to do with the product.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 10 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #D-296-2013 (February 11, 2013) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-296-2013 to see it in context.
- Plain-language summary written by qwen3.6:35b-a3b on October 13, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.